| Tag | Content |
|---|
EnhancerAtlas ID | HS105-85429 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chrX:129254280-129255460 |
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 | CTAGATCCGG ACTTAAGCAG AGCCTCTACC TCTCATGTCG GCCGAGCCGA GTCTCAGGCT 60
GCGCCCCAGC CTTGGCCACA GTCTGCATCC CCTGTGCTGG AGATGCGTTC TAAGTCTCAT 120
GGGAGCCAGG CTAGAGAGTG GCTGTTCAGG GAAACCCACC CCCAACGCCC CAGACACGAC 180
TCAAAGTTTC CATTCTACTG CCTGCGGGTC AAGAGCGCCA TCCCCAGAGA GCAAAGACCG 240
CCCGAAACTG CAATTCCTTT GCTGAAGTTA GGAGCCGCCC GGGGCTCTGT GGGGCCTGCG 300
AGGTGGCTCG AGGGACTTTG CAGAAGCGCG CAGGAACCAG CCCCCGACCT GGGGCGCTCG 360
GCCGCGGGGC TGATCTCCGT ACTCTCCCGC CAGTGGGGTG GGAGCGCGTC CTTCTCTCGA 420
GTTCGGGGAC GGCCTGAGAA GCAGCGGGGG CTGGTGGCCT TTTTCTCGCT ACCCCCTTTC 480
TAGGCTCGCG CGCCTTCCAA GCCCGGATCC TGGTGGGGCT GAGCGTGCCC ACCCGCCCAG 540
CAGTGCGCCC GGGCGCCTCT GCAGCGCCAC CTGCACGCGG AACGCGGCGG CGGCGGCGGG 600
AACTGTCGTC CAAGGAGGAG CAGCAGGAGG AGGAGATATC GGCTCCTCTG CCCCCAGCTT 660
TCCTCGCTGG CACGCGGCCT CCCTTCGCCG CCTCAGCCCC AAGCGGCCTG ACCAGCCCAG 720
CCCCAAGCCT TGTCCCGCGC CCTGCCCGGC GCAGGCAGCC AGCGCCCCGA GCTTCCACTC 780
CTGCTGCTGC GCTCTGAGCG GCCTCCTGCC CTGGGCGCCT CTTCTGGGGA AGCAGTGAAG 840
TCACACTGGG CCGGATCCGC TGACTCATGA GAATGAGACT CTTCCCCGGT CCCCGGCACA 900
CCCTTTGAAA CTTCCCCTCA ATCCTTTCTT TTTTTTCTTT TCTTTTCTTT TTTTTTTTTT 960
TTTTGGCGGA GTCTCGCTCT TTCGCTCAGG CTGCAGTGGC GCGATCTTGG CTCACTGTAA 1020
CCTCCGCACC CCACCCCCGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCCG GAGTAGCTCG 1080
AATTACAGGC GCCCACCACC ACGCCCAGCT AACTTTTGCA TTTTTAGTAG AGACAGGGTT 1140
TCACCACGTT GGCCAGGCTG GTCGCGAACT CCTGACCTCA 1180
|
