| Tag | Content |
|---|
EnhancerAtlas ID | HS184-19125 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr21:46806080-46807680 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr21:46806852-46806869 | AGGGTCACCGTGACCTT | - | 8.64 | | ESR1 | MA0112.3 | chr21:46806852-46806869 | AGGGTCACCGTGACCTT | + | 8.87 | | ESR2 | MA0258.2 | chr21:46806853-46806868 | GGGTCACCGTGACCT | - | 7.2 | | ESR2 | MA0258.2 | chr21:46806853-46806868 | GGGTCACCGTGACCT | + | 7.52 | | PPARG | MA0066.1 | chr21:46806850-46806870 | CGAGGGTCACCGTGACCTTG | - | 6.21 | | PPARG | MA0066.1 | chr21:46806851-46806871 | GAGGGTCACCGTGACCTTGA | + | 6.36 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_44555 | chr21:46806116-46807932 | NHDF-Ad |
|
| | 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 |
| GH21I045385 | chr21 | 46805134 | 46808785 |
|
Enhancer Sequence | CCCAAAGTCC ATCTTTCCCC CAGATGTCAT CAGTGCCTGC TTCCCTCCCT GTGGAGGGCT 60
CTGAGGGCCG ACCCCCAAAG TCCATCTTTC CCCCAGATGT CATCAGTACC TGCTTCCCTC 120
CTTGTGGAGG GCTCTGACGG CCGACCCCAG GGTGGGAGAG GGCCAGCCCC CCAGCAGCAG 180
GAGCAGTTTA AACTGCGGGT AAGTGTGCTC CAGGGGCCCT GGTTCTGCAG AGCCACACGC 240
CGAGGCTCCT GAGCTATGTG AGGAATCCAG GGTGCAGCTC ACTGCGTGTC GCCCAACTGC 300
CCTGGGAACC GGCACTGCAG GGTCAGGTGC ATCCCTTTCC ATGTGAGCTC CTGGCCAGCC 360
CAGGCAGACA GGGGAGGCCA CACAGCTTCC AGGCAGGCAG CGGCTGGGCC TGAGCTGGCC 420
CATACCTGCC GGGCTCCTGT CCCACCGGCT GTGTCCGGCC AGCCAGGGCT GGGGACATAC 480
ACACCTGAGC TGCTCTCAGG AGCACTTTTA CTGGAACCTC GAGGAACCTC AACCTCCTTG 540
TTTCTAGGTT GCAGCTCCAT TACGTGCTCT GCAAGTGAAA GATGCTGAGG TGGACACTAA 600
CGTCGGGAGG GAAGCCTAAA CATTGACGTC ATCTGTGCAA AAAGTCAGGA GCATCCACAG 660
GTCCACTCTG TCCCGGACAC GTTCTCAAAG TCAGGAGCAT CCACAGATCC ACTCTGTCCC 720
GGACACGCTC TCACGCTCTC TCCGGTTTGA CTTTGCAATA ACACAGCCCA CGAGGGTCAC 780
CGTGACCTTG AAACAGTCCT GGCTACTTTA AAATTAGCTG CCCCTAGGAG CATGGAAGAT 840
GATTCATCCC GTGACAAATC TTGCCTTATG TCTCTTTTAA ACACACACAT CTGGGTATCA 900
GGCAGCCTCA CGGGGGCAGC TTGGTTGTGC TGGAACTCAG CCTCATTGAC TCCGGTTTCA 960
TGTGCACAGA AACTGACTTT GAAACTTGCA GGAAGAGGCT GTCCTGGAAG AAGCTGCAGC 1020
CTGCAGAGAC GGCCCTGGGC TTCCTGCATC GCTCCCTTCC TGCCACGGGG CTGTGCCAGG 1080
AGCTTCCATG CAGCTCTCAC ACACAAGGCA GGTCCCCAGC TGGCTCTCTG CAGAGCCTGA 1140
CCTGAGGCAC CCATTCGATG AGAGCAGGTT CTCTCAGTGT AGAACCCAGA CCAGCAGAAG 1200
CCGCATCACA GGGACGCTTC AGAGACGCAC TGCTCAGCCC AGAACTGCCA GGCCTGGCAG 1260
CCGGGGTGCG GGGACCCTGG GACCCTGATG TTGTGTGAGT TCAGGAAAAA CAGCGTTGCC 1320
TTCCTGAATG CTGTTCCATT TACTTCTAGC TCCTACGTGT TTCTTCAAGT AAAACACAGT 1380
CGAGCCTCAT TATTCATGGG CAAATTTGCC TACTTACTAG CATTTACCCT AACCCAGATT 1440
CAATACTCAG GGCACCTCCA CGGTCATTGG TGGACGTCAC AGCGTCACAG CAATGAGACG 1500
TGAGTTTCCT GACACGGTGT CTGGGCGGGG GCAGAACGAG CCATGCTTTG GTGTCTCGTT 1560
TGTGTGTGCG TGAGTGTGTG AATGTGGGAG TATGTGAGTG 1600
|
