| Tag | Content |
|---|
EnhancerAtlas ID | HS003-49444 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chrX:129254140-129255450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chrX:129254896-129254917 | GGAGCAGCAGGAGGAGGAGAT | + | 6.5 | | ZNF263 | MA0528.1 | chrX:129254893-129254914 | GGAGGAGCAGCAGGAGGAGGA | + | 8.06 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_24424 | chrX:129254766-129255163 | Colon_Crypt_2 | | SE_32136 | chrX:129254163-129255263 | Gastric | | SE_50613 | chrX:129252083-129255264 | Sigmoid_Colon | | SE_53216 | chrX:129254291-129255256 | Small_Intestine | | SE_54074 | chrX:129254305-129256027 | Spleen |
|
| | 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 |
| GH0XI130117 | chrX | 129251568 | 129256117 |
|
Enhancer Sequence | GAAGACAGAG GTTGCAAGTT TGAGCCCCAG ATAAGCCCTT AGTTTTTTGT TTTGTTTTTT 60
TGTTTTTTGT TTTTTTTTCT TTTTTCCTTA TATAGCTGCA GAAGACCGGA TTGACAAGCA 120
CGGACCACCT AACTGTCCCT CTAGATCCGG ACTTAAGCAG AGCCTCTACC TCTCATGTCG 180
GCCGAGCCGA GTCTCAGGCT GCGCCCCAGC CTTGGCCACA GTCTGCATCC CCTGTGCTGG 240
AGATGCGTTC TAAGTCTCAT GGGAGCCAGG CTAGAGAGTG GCTGTTCAGG GAAACCCACC 300
CCCAACGCCC CAGACACGAC TCAAAGTTTC CATTCTACTG CCTGCGGGTC AAGAGCGCCA 360
TCCCCAGAGA GCAAAGACCG CCCGAAACTG CAATTCCTTT GCTGAAGTTA GGAGCCGCCC 420
GGGGCTCTGT GGGGCCTGCG AGGTGGCTCG AGGGACTTTG CAGAAGCGCG CAGGAACCAG 480
CCCCCGACCT GGGGCGCTCG GCCGCGGGGC TGATCTCCGT ACTCTCCCGC CAGTGGGGTG 540
GGAGCGCGTC CTTCTCTCGA GTTCGGGGAC GGCCTGAGAA GCAGCGGGGG CTGGTGGCCT 600
TTTTCTCGCT ACCCCCTTTC TAGGCTCGCG CGCCTTCCAA GCCCGGATCC TGGTGGGGCT 660
GAGCGTGCCC ACCCGCCCAG CAGTGCGCCC GGGCGCCTCT GCAGCGCCAC CTGCACGCGG 720
AACGCGGCGG CGGCGGCGGG AACTGTCGTC CAAGGAGGAG CAGCAGGAGG AGGAGATATC 780
GGCTCCTCTG CCCCCAGCTT TCCTCGCTGG CACGCGGCCT CCCTTCGCCG CCTCAGCCCC 840
AAGCGGCCTG ACCAGCCCAG CCCCAAGCCT TGTCCCGCGC CCTGCCCGGC GCAGGCAGCC 900
AGCGCCCCGA GCTTCCACTC CTGCTGCTGC GCTCTGAGCG GCCTCCTGCC CTGGGCGCCT 960
CTTCTGGGGA AGCAGTGAAG TCACACTGGG CCGGATCCGC TGACTCATGA GAATGAGACT 1020
CTTCCCCGGT CCCCGGCACA CCCTTTGAAA CTTCCCCTCA ATCCTTTCTT TTTTTTCTTT 1080
TCTTTTCTTT TTTTTTTTTT TTTTGGCGGA GTCTCGCTCT TTCGCTCAGG CTGCAGTGGC 1140
GCGATCTTGG CTCACTGTAA CCTCCGCACC CCACCCCCGG GTTCAAGCGA TTCTCCTGCC 1200
TCAGCCTCCG GAGTAGCTCG AATTACAGGC GCCCACCACC ACGCCCAGCT AACTTTTGCA 1260
TTTTTAGTAG AGACAGGGTT TCACCACGTT GGCCAGGCTG GTCGCGAACT 1310
|
