| Tag | Content |
|---|
EnhancerAtlas ID | HS184-31991 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chrX:13025910-13026730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chrX:13026636-13026647 | TGCTGTTTACA | + | 6.14 | | MEF2C | MA0497.1 | chrX:13026450-13026465 | GAAATAAAAATAGCA | + | 6.07 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_31989 | chrX:13026046-13026885 | Gastric | | SE_32462 | chrX:13015228-13027887 | GM12878 | | SE_49904 | chrX:13025264-13026748 | RPMI-8402 | | SE_50189 | chrX:13025347-13027492 | Sigmoid_Colon | | SE_58417 | chrX:12964783-13034394 | Ly1 | | SE_58905 | chrX:12964721-13049077 | Ly3 | | SE_62231 | chrX:12964510-13049336 | Tonsil |
|
| | 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 |
| GH0XI013004 | chrX | 13022555 | 13027118 |
|
Enhancer Sequence | TCTAATAAGC TCCCAGGTGA TCCTGGGGTT GCCAGTTCAC AGACCACATT TTGGGTATTG 60
AAAGTCTAGG TACCTCTGCT AGTTTGCTGA ATGCAACTGA GAAAGAAACC TCAGGGTTAA 120
TGCTTGCATT TTTCTGTCTT CATTTCTCCA TTGTCCTACT CTCCTCCCTT GGAAGGCTCC 180
AGCTTAGAAA AAGAAAACAT TATGAAATAG CAGTGCCAAA CCTGAATTAC AATGTTAGGC 240
ATGTAATTAT CTGGGCAAAA GCCAGATGTC TCAGACTAGG GTTTAGTACA GCTTGCCAGG 300
GCTGGGTAAA GTTCCTAGAT TGAAGACACA GTTGAGACTA CATGACATAT GCAAGAGAAA 360
AGGGGTACCT GTGCCTGAAA CTCTGGGAGG TGAGAAGTGG ACAAGGGTTA CTGCTGCATA 420
AGTAATTGAG GAAGCTTCTC CTTCCCCACC AGACTGCAAA CTGAGATGTT TGCATATTAA 480
TCTTGGCCAC AGGGGTGACT CGGTCTGTGT CTGCAAATGA AAGGTTTCAT CCTTGGCTGT 540
GAAATAAAAA TAGCAAATAG CATGTGGCAT GCAGGGGCTT TTCCTCTATA AGGGGCTGTC 600
ACTGTCCACT GTTTAAAGCC TCTGCTTGAG CCATCTTCAA GGAAGGAGGG TTGTGAATGA 660
GTGGGGGCAG ATTGCAGAGC CAGTTCGTAG ACAGCAGAGA TGCTCCAGGG AAAACCTCCC 720
TTCTCTTGCT GTTTACATTT GCACATACTT ACCAGTTTGC CAGAACTTCT TGGTGTCAAC 780
AACTTTGACT GAGACTGCGC CACGTGAATG TATCTCCTGG 820
|
