| Tag | Content |
|---|
EnhancerAtlas ID | HS184-22495 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr4:6634630-6635770 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr4:6635267-6635279 | TGCCCTGGGGCT | - | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 6635356 | 6635560 | | chr4 | 6635400 | 6635627 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH04I006632 | chr4 | 6633843 | 6636132 |
| Enhancer Sequence | CCACCATGCC CGGCCTATAC CCACTTTTAA TTATGTGAAA ATTAAGGGGG GAGATTATAC 60
AGAAATTTCT AGAAATAGGG TGGTAACTTC TGGGTCATAA GGCTGTTGTC ATGGAAAGTG 120
GCAGTAATGT CCGGGTGTTG TCAGTGGGCA TGGATTCTGT AGAGGTGCTT TTACCTCTTC 180
CCCTGTTTAG CTAGTCCTCA GACTGGTCTG ATGTCTGAGC CCTGTCTCCA GAGTCCCGCC 240
TCCTGCCGTC TCACTAGGAC TACACATGTG CAGGCAGCTC TAATCCTTCC CTGGAGGCCG 300
CCCAGGTGTC CAGGGGCTGT GCTGCCTCTG GGAATCATTA AAGGTCGCTC TGTGCCCAAA 360
GCCTCTCACA CTGGGCCCTC AGCATCACGT CCTCTCCCAA GAGGGAACAA AACAATCCCT 420
TCTCTGCTCT ACTCTGCAGA ATTTACAGCT GAGCCATAGG ACTGGGAGTT CCAATTCTTC 480
CCCCATGTCG CCCTGCCTTT CATCACTTGG TCCAGGACAA ACTGTTCTCC AATTTCCAGC 540
CTGGGGAAAA GCAAGTTCTG CCTCATGGCA GCATTTACCA GCTGAAACGC CCTGGTTTTG 600
TTTGCACCTG TGTTTGTTCT CAGGCTACAG CTAATGATGC CCTGGGGCTG CCCACAGTCA 660
AACTGGTTTG CAAAATTGCA TCTTTGACTT CAACAATTTC TAAAGAATCT CTAAATTTAT 720
AAATAATTCA CTCAAGAGAA AGAAAAATGA ATCCAGACAA ACTCTGCAAT GCACCAAAGA 780
AATGGAATCT ACATAGAGAT TGCACTATAG GTGAATGAGG CAAAAACAGG AAGCTATTGC 840
AACATTGGGG GAGGCGGGAG TTGGTGGATG TGCATAAAGT CCTGGTCCCA GCCTTACAGA 900
ATGCTCACTC TTCTCAAGCA CACACACAGA GTGTGCTGCA ATTGCCCAGG CCGAAATTTT 960
TACAAATTTC AGAGAATCAC TATCAAACCG AACTCCATCT CTAAGAAGAA TACAATTAAG 1020
TTAGACATCA GTAATAGAAG AGCATAAACA GCTCTAATGT GGTTGAAATT TTTAAAACAC 1080
AGTTTTGGGT TTTTTTTCTG GTTTTTGGTT TTTTGTTCAT TTGAGACAGA GTTTCGCTCT 1140
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