| Tag | Content |
|---|
EnhancerAtlas ID | HS184-04396 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:95048470-95049430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr10:95048979-95048998 | TGCTGCCATCTTGTGGACA | - | 6.83 | | YY1 | MA0095.2 | chr10:95048980-95048992 | GCTGCCATCTTG | - | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_32827 | chr10:95048520-95049016 | H1 | | SE_68917 | chr10:95048319-95049647 | H9 |
|
| | 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 |
| GH10I093287 | chr10 | 95047101 | 95049568 |
|
Enhancer Sequence | AATTTCTATT CCTTCAAGTT CCCTGCCACT CCTGTCCGTA TGTACAGCAG AGCCAATATG 60
GACATCCCGT CACAAGGTCT GTTTTCCTTT GCTTAACCTT CAATCCTGTA TTATGACAGT 120
CTGCAGGCTT GTAATTTTTC GTTGCATGAG AGACTCCTTC CTGTGATCTA CCACTGTTTG 180
ATTTGCGACT CGCTATGGGT CATGAGAGCA GGCCCTTCTG TTTTATTCCT TTGCAGGATA 240
ACTGGGATGC GGTAGGCTTT TAGTACATAA TTGTTGAAGG AATGAAGGGG CGAATGAATG 300
CGTGAGTTCC AGCGTTTCCC AAGGCCAGAG CGTTTTTGTC TGTCTAGTCA TAGATTTCCA 360
TAGCATTCCA GAAGGAAGGG CATCGTTTAG ATGCGGTGCT GGTCGCCTTC CACTTAAAAT 420
ATGTCCCAGA GATGCCTGTC TGGGGTGGGG TTCCATGGAA TGCAGACTGA ATGGAATGCC 480
TTTTAGGCCC GGTGAGAACC TGAGGCCACT GCTGCCATCT TGTGGACAGT ATTTGAAACA 540
CAGGAGACGT GATGGCCGTT TCTCCCAAAG AAACCTTGGC TGATTCTATT ACATGATGAA 600
ATATTCTCCT TAGCAGTGCA TTAGGCCATG TTACCAGACC CATCCTTAAC CTATTTGTAT 660
TCCTCTGTTG AAATAATAAT AATATAATAA CAACAACAAC AATAACTCCC ATTTGCTGAG 720
TTTTAGGCAC TGTGCTAGTA AGAGAACCAG GATTTGACCT CATCCCATCC ACTCTGGACC 780
CAACTTTTGG CCATTTCCCC ACACTCTTTC GTTTTTTGAG TTCTTTCTCT TCTTTCCCTT 840
CCAACTCTCT ACTGTGATTA TGTATCAGTC CCTGTAGTCA CATCTTGTCT CAATGATTTG 900
CTTATGTGTT TGCCTTTCCA ACAAGACAGT GACCACCTTG ATGACTGGTC AGAGCTGTTG 960
|
