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EnhancerAtlas ID | HS183-10665 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr7:142571460-142571820 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr7:142571491-142571507 | GGTTACCATGGCAACC | + | 7.99 | RFX1 | MA0509.2 | chr7:142571491-142571507 | GGTTACCATGGCAACC | - | 7.99 | RFX2 | MA0600.2 | chr7:142571491-142571507 | GGTTACCATGGCAACC | + | 8.31 | RFX2 | MA0600.2 | chr7:142571491-142571507 | GGTTACCATGGCAACC | - | 8.35 | RFX5 | MA0510.2 | chr7:142571491-142571507 | GGTTACCATGGCAACC | + | 8.42 | RFX5 | MA0510.2 | chr7:142571491-142571507 | GGTTACCATGGCAACC | - | 8.51 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATAGAAGGC TGCTCCACCC AAGGGGGTGA GGGTTACCAT GGCAACCATG CAGACGACCA 60 GCCCACCCCG GGCTCTGCGT GCATGTCCAT CCTGGTCCCT TCATCTCAAT ATCACCAGCT 120 CTGCAGTGCT CCAAACTTTG GGTTTTTACG GTCCCTAGTT TTGTATGAGC CTCATCTTGA 180 TCCTAAGAGC CACCTCTCCC TAACACTCCC GATTTTTCTC ACCTCTGGAG GACGTCCCAT 240 CCTCTGATAC CATAGGTCTC CTCTGATCTC TGCATTACTC CTCCTCCCCA AGTTTAGCCA 300 GAGCCAGTGC CCCCTAGACT TCCTCATCTC TTCCCTGCCA TGGCCCCTGG TCCTGGACAG 360
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