| Tag | Content |
|---|
EnhancerAtlas ID | HS197-04278 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr11:110236740-110237780 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr11:110237088-110237106 | AATATGCTGAGGCATGTT | + | 6.19 |
|
| | 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 |
| GH11I110365 | chr11 | 110236541 | 110237628 |
|
Enhancer Sequence | CCGAGTAGCT GGGACTACAG GCTCCCACCA CCAGGCCCGG CTAATTTTTT GTATTTTTTA 60
GTAGAGACAG GGTTTCACCG AGTTGGCCAG GATGATCTCA ATCTTCTGAC CTCATGATCC 120
ACCCGCTTTG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGTG CCCGGCCCCT 180
GTTTCCATTT TTTGGGGTGT ACACCCAGAG GGGGAATTGT TGCATCACAG GGCACTGGCA 240
TTTAAATTCT CACTCTTCTC ATTTGGTGTC TCACACCAGT TTGCATTCCT GTTTGAGCGA 300
ATTTGTAAAT CACATACCAT ATTTGTTTTC TTCTCTGTTT CACAGATAAA TATGCTGAGG 360
CATGTTTTCA AGGAGGGGAG AGAGATTCCT TTTCCTCAGC CGGGCACAGA GCCAACCTGA 420
AGTGTAGCAC TGTGGTGACC TGGCGGGATC TGCTCTCCAG TCACTCCCGA GGGCCCTTCT 480
GGGGACAAGG AGACTTTTCT GTGCGGCCTG TTGATTTGAG TAGGTATAGC CTTTCTGCTA 540
GCCACCAGAC ACAGCTCTAT AAGAATTTAC TCTCAACTAT CCCATGAATA AGAAAACACT 600
TAGGGAGGCT TTTACCTATC CATGAATAGT TACTTCTGTT CAACAGTCCT ACAAATGTTT 660
TCGAATGCCT GAAGTGTGCC AGACATGTAC TAGGCAACAG GGTTAGAAAA GTGTGGGAAG 720
CTTGGTCCCT GGCCTGGAGA ACTTTAGTTC AGTGGGGAGC TTACAGATAT TCCCCCCATA 780
CCTTTCAGAG CATGGATGTT TACAAAGTTG TCAAAGAGTA TTTTGGTGTG CTTTGGCAAT 840
GGTGGATCTA GTGTTGTGGG CCTTCTAAAA ATATGAAATG ATGAATTCAC AATTAGTTAT 900
AAGGTTTTGA AAGGGATTAA TACAAATGGG TGGGGTGGGG TGGATGGGAG GAAGGTCCTG 960
AAATAGTTTT ATTAACTTGG TAGTAAATAA TTTCTGGATT TGAGGAGTAT TAAAAGGATC 1020
CTTCACTCCC AAACCTCTCC 1040
|
