| Tag | Content |
|---|
EnhancerAtlas ID | HS095-06097 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:110236610-110237540 |
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 | CTGCTTCTTT TTTTCTTTTT TTTTTGAGAC GGAGTCTCGC TCTGTTGCCC AGGCTGGAGT 60
TCAGTGGCAC GATCTCAGCT CACTGCAACC TCCGCCTCCC CAGCTCACAC CATTTTCCTG 120
CCTCAGCCTC CCGAGTAGCT GGGACTACAG GCTCCCACCA CCAGGCCCGG CTAATTTTTT 180
GTATTTTTTA GTAGAGACAG GGTTTCACCG AGTTGGCCAG GATGATCTCA ATCTTCTGAC 240
CTCATGATCC ACCCGCTTTG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGTG 300
CCCGGCCCCT GTTTCCATTT TTTGGGGTGT ACACCCAGAG GGGGAATTGT TGCATCACAG 360
GGCACTGGCA TTTAAATTCT CACTCTTCTC ATTTGGTGTC TCACACCAGT TTGCATTCCT 420
GTTTGAGCGA ATTTGTAAAT CACATACCAT ATTTGTTTTC TTCTCTGTTT CACAGATAAA 480
TATGCTGAGG CATGTTTTCA AGGAGGGGAG AGAGATTCCT TTTCCTCAGC CGGGCACAGA 540
GCCAACCTGA AGTGTAGCAC TGTGGTGACC TGGCGGGATC TGCTCTCCAG TCACTCCCGA 600
GGGCCCTTCT GGGGACAAGG AGACTTTTCT GTGCGGCCTG TTGATTTGAG TAGGTATAGC 660
CTTTCTGCTA GCCACCAGAC ACAGCTCTAT AAGAATTTAC TCTCAACTAT CCCATGAATA 720
AGAAAACACT TAGGGAGGCT TTTACCTATC CATGAATAGT TACTTCTGTT CAACAGTCCT 780
ACAAATGTTT TCGAATGCCT GAAGTGTGCC AGACATGTAC TAGGCAACAG GGTTAGAAAA 840
GTGTGGGAAG CTTGGTCCCT GGCCTGGAGA ACTTTAGTTC AGTGGGGAGC TTACAGATAT 900
TCCCCCCATA CCTTTCAGAG CATGGATGTT 930
|
