| Tag | Content |
|---|
EnhancerAtlas ID | HS184-06659 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:117381380-117382860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RAX | MA0718.1 | chr11:117382577-117382587 | GTTAATTGGC | - | 6.02 | | TP53 | MA0106.3 | chr11:117382650-117382668 | CACATGTGCAGGCATGTT | - | 6.48 | | TP53 | MA0106.3 | chr11:117382650-117382668 | CACATGTGCAGGCATGTT | + | 6.4 | | ZNF263 | MA0528.1 | chr11:117382375-117382396 | CTCTCTCCTCTCTGCTCCTCC | - | 6.78 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I117510 | chr11 | 117381527 | 117384259 |
|
Enhancer Sequence | GCAGGGATTT TTGTCTATTT TGAGCATAGC TGTATTCATA GAACCTAAAA TAGTGCCTGG 60
AATCTAGTGG AGGCACAGTA GATGTCACTG AATGAATGAC ATTCGTGGTC ATTATCCTCA 120
TCACCACTAC CATCGTCATG AGCCCTGTCT GTCCCACGGG AGTTTGCTTC CTCCTTTGTT 180
ACTGGCTCCC TTGGCTGAGG AAGTAAGGTT GTTGGCAGTG GCTTCCTTGG TGTTCCTCCC 240
CCAAATGGCA TGCAGGCCAT CTCCTCCTAG GGAGCCTGCT GTGCCCCTTT CCTGTGGATC 300
CCAGTGAGGT TCCTCCCAAA TCTCCACCTT CACCAGTAGC AGGCACTTGG CCAGGTGGCT 360
GACTCTCCCT TAAGCTTATC ATCATAGAAA CCCCCAACCT ACTCGTTAGG GTGGGAGAGG 420
GTCTCTGGCA CATGCTCCCA GGCATACGGC AGAGGCTGGG TGGAGCAGTG CTGAAGCTCA 480
GCATTGAACA GCTAGGGAAA AATTAGGGAG GGAGGAGGGA ACATGGGCAT TTGGGAGAGA 540
GGGTGTTTGT GTGTGGGTGA GTATGTCCCT CTTCCACTTG TCCTCCACAG AAGCCTGGCA 600
CCACCTCCCT GTCCTGGTCC TGCTGAGCAT GGGCAGAAAG CACCTCTTGG CCTTGTTTTG 660
GCTCAAGAAG CCCTCGGAAG CTCAGATGTA GGAATGGAGA TGTTTCTTCA CGGAGCCAAT 720
GCAAAGGGGC CCCAGTTGCA GCCCTGCCTT CCTAGTTAAT TAAACATTCA GCCTGCATGC 780
CCAGAGATGC TTTTGTGCTA CATTATTTTT CAGCTACAGG TGGCCCTAAA GTCACCAAAT 840
CTAGGTTTGA TCTGTGTGCT CTCCTCTTAG CATCCTGCCA AGGATTTCTC CGGATGACCA 900
GAGACAAATA CCAGCCATCC CTGCAGCCTG GCTCTCCACT GCCAGCCAGT GTCACATATG 960
CCAAGGCACA CACAGCCTTC AAAGCACCCT CCACCCTCTC TCCTCTCTGC TCCTCCCACT 1020
TTACTGGAAC ACAGCAGGCT CCCTTGGGCA ATATTTCATA TGGTCCCACC TGCAGCCACT 1080
TTTTGGGCTC AGGAATGTTG CCTTACGGGA GGGCCCTGGT GGACAACACA CTTGCGTATG 1140
TGTAACTGCT GGCATGCATG TTTACGTATG TGTGCTCAAG TGTGAATGGG CTAATGTGTT 1200
AATTGGCTGC ACGTGCATGC AATACGTACC AGGGTGCACA CGCACGAGTG CTCACACACA 1260
GGTCTCTGCA CACATGTGCA GGCATGTTGG GCGTGTGCTG CTGTTCGCAG CTTAGTGTTA 1320
GAAAAATTCG TTAGAAGACA AGCAGTCCCA GAAGGAATGG AGTCAGCAGT TGTTTTTCCG 1380
GCTCATGGAG CAGCATGGGT TTCAGCCCCA CCCTGCCCAC TGACCCTTGG CCCCACAGAG 1440
AGCTGGGGTG GGAGACTTCC AGTTTTATCT CACACTTCCG 1480
|
