| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10020 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:57304160-57305110 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr11:57304332-57304350 | ACCATGCCCAGGCTTGTT | + | 6.21 | | ZNF263 | MA0528.1 | chr11:57304980-57305001 | GAGGGAGAGGAAGGGGGGAGG | + | 6.34 | | ZNF263 | MA0528.1 | chr11:57304973-57304994 | GGTGGAAGAGGGAGAGGAAGG | + | 7.27 | | ZNF263 | MA0528.1 | chr11:57304976-57304997 | GGAAGAGGGAGAGGAAGGGGG | + | 7.27 |
|
| | 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 |
| GH11I057536 | chr11 | 57304032 | 57308087 |
|
Enhancer Sequence | TCAGCCTCCC AAGTAGCTGA GATTACAGGC ATGCGCCACC AAGCCCGGCC AATTTTTGTA 60
TTTGTAGTAG AGACAGGGTT TCACCCTGTT GACCATGCTG TTCTTGAACT CCTGGCTTCA 120
AGCAATCCAC CCGCCTCGGC TGCCCAAAGT GCTGGGATTA CAGGCATGAG CCACCATGCC 180
CAGGCTTGTT TTGTTTTTTT CTTAGCAAAA TGTCAGTTCA GTATAAAAAT GTGTTCAGAG 240
CCTACTGTGT ACCTGTCACT TCAGCTCAAA ATAGAACTCA GGAGTTTTGT ATTTTCCAGG 300
CTCCGTCCAG TGATCCGTCA GCTTGTCCCA TCACTTTTGC CCTCTCTGCC CCTCCCCCTC 360
CAAATCTCTC AGTCAACTGT GAGCCCCAAG ACACATCCCC TGTGTTGGCA GCTGCCCTAC 420
TCGCCCCCTC CTTAGCCCAG CCTTAAGCAG CTGCTTTTGT CTGAGGACGA GGGAAAGGGG 480
CTATGTAAGG AACGTGGCGG GGTGGGTGTG AAGGGAGCAC AAGAGGCCTC GCCTGGGCTC 540
TGGATGAGCA GTGGAGGCCA GGGCCATGCT CTAAATGAGT CCTGAAGATG GTTGTCAAGG 600
TCCCTAGGGT TAGGAGAGTC CACTGGGGAG AAAGATGACC ACAGGACGGA TGCTGCCAGG 660
CTCAGGGCGG AAGGGACGTG CCGTGATTGA AAGGTGCCAC CTGTCAGATC TTCCACGGGA 720
AATCCGAGCC TCCCAGTCTA GGGTAAAGTG TTGTACCAAC AGGCCAGTAA ACAATGCTCT 780
TCAGGCAGCC CAAGACTCTT GAAGTGGGGG TGGGGTGGAA GAGGGAGAGG AAGGGGGGAG 840
GCGGGACCAA AGAGCTGGGG GCTAGAGGCC ACTGGGGCTT AAAGGCAGCC TGGGAGTGAG 900
GCCACTCAGC TGGAGCAAAG AGACAGCTCC CAAGCCACAG GCAGAAGCCC 950
|
