Tag | Content |
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EnhancerAtlas ID | HS184-04241 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:86024290-86025180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr10:86024517-86024536 | GTACCACAAGGTGGCAGTG | + | 6.1 | FOXC1 | MA0032.2 | chr10:86024391-86024402 | TATGTAAATAT | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I084264 | chr10 | 86024441 | 86024630 |
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Enhancer Sequence | TCTGCTGTTC TCCCTGTCAG AGATACTCCT GGTCCAATTC TCTCAAATAC AAGCTCACTC 60 TCCTTCCCAC CACAACTGTC TCCCTTCTTG TGTTCCCTGT GTATGTAAAT ATCACTATTA 120 TCTGTCCTGT CATCTAAGGT AAATGAAGAG AGAAGGGAAA AGCAGAGATC CGACATGCAT 180 AAATACTCGC ACTGGGCAGA ATGTGAGGGT GGCGCAGTGC TCAGCAGGTA CCACAAGGTG 240 GCAGTGCCCT CTCAATGATC AGTACATCCT GAGCTGCCAG CCCTGATGGT AGTGCCTCTC 300 CGCAGAGCCT GGGGGTCTCC TGCTGAGGCC GCGTGGGTGG GTTATTGATT CCTGCAGGAT 360 TTCCGACACG TTTTCCTTTG CCTGCTCGTG ATACAGACGA AACCTGACAC TTAACTGTTT 420 CTACCTCAAA TGATGACATG ATTCCACATC TCTCTCTTTC TTAAAGGAAA CACAGTGTCA 480 TGCACGTTGG CCAGAGGAGT CTTTGATGGC CCCATGGAGT CAGTCCCTTT TCTCTGTCTA 540 TAGAACAGCC ATTGAATGTC TAGCCAAATG GAGGCCTCCA AAGCCCTGCA CACCACAGCA 600 TTTTGATAAG AGGTCTGGGC CTGGGTTTTG TCTTTGTCTG ACTGATAAGT CAGGGCAGTC 660 CCTGGATTTC TCCAACCTGG GACTGTTCAT CTGAAAAGTG GTGGTGATTA GCCCTCATGC 720 TGTGATCATA GGTGGAAGAA CACTGCAAAC TATGGGGTGT GGGGCAGGAG GGTTCGGAGA 780 AGCACCCCAC TCCTCAGGCA GAGGCACAAT AAATGACATT TGGCAATTGT GGGCAATGTT 840 TCTAAGGTAA CGAGGGCTGG GAAAGCACTG GGTGAAGGCC AGAGATATAA 890
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