| Tag | Content |
|---|
EnhancerAtlas ID | HS184-32455 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chrX:154624520-154625030 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chrX:154624817-154624835 | GACTCCTTCCTTCCATCC | - | 6.32 | | EWSR1-FLI1 | MA0149.1 | chrX:154624821-154624839 | CCTTCCTTCCATCCCCCC | - | 6.73 | | NR2C2 | MA0504.1 | chrX:154624914-154624929 | TGCCCCCTGACCCCT | - | 6.54 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGAAAAAAAA GGCCATAATA AAGAGGGCAA AGGACATGAA TGGACACTTT TCAAAAGATG 60
ATATATGCAG GGAGCCGAAG GCCCCGTGGG ACGTGACCAA CTCAGCATTC CACTGGAGGC 120
TATATGATCA AACAGCAAAC TGTTTATGAT GAATGCAGGA TGTGGGCAAA CTCACGACTG 180
CTCCCGCTGC CAGAAGGTTT GCTGAGGGCA ATCGCTTCCT GGCACGAGCT CCTTGAGGTT 240
ATCTACTGGG ACATCTAGAG AATGCAGTCT TGCAAGCCTA CTCTGGACTG AGCAGCTGAC 300
TCCTTCCTTC CATCCCCCCT TCTCACTATC TCTTTTGCCT AATAAATACA GAGGGCTATG 360
TAAAGCTCAG GGCCCTTGTC CACTAGAGGC AAGGTGCCCC CTGACCCCTT CTTCCAAAAA 420
TACTCTTTTG TTTTTGTCTT TTATTCCTGC ATTTGCCCTC TTTGTTCAGT CCCCCTAGTT 480
CTGTGCAGGT TACAGACATA CATGCAGCCA 510
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