| Tag | Content |
|---|
EnhancerAtlas ID | HS138-40499 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr8:38377590-38378560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr8:38378452-38378463 | TATGACCTTGA | - | 6.62 | | EWSR1-FLI1 | MA0149.1 | chr8:38377816-38377834 | GGGAGGAAGCAAGGAGGA | + | 6.35 | | EWSR1-FLI1 | MA0149.1 | chr8:38377812-38377830 | GGATGGGAGGAAGCAAGG | + | 6.98 | | Esrra | MA0592.2 | chr8:38378453-38378464 | ATGACCTTGAC | - | 6.32 | | Esrrg | MA0643.1 | chr8:38378453-38378463 | ATGACCTTGA | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGCCTGGGCA ACTGCCTCAA AAAAATATAA AAATAAAAAT AAATAAATAA AAAAGAGAAC 60
TAGAATCCTG ACTGTGGCCT AGAGATTTTT TCCTCCATCT CAGTGACTTG GCTCATATTG 120
GTGACTTTGC TTTTTTCTCT CAGGCAGATG TGCTGCTTTG AACTGGGTGA GTGCTCCCTC 180
CTGGTGAGGA ATATGCTGGA GCTGGGGTTG GGCAGCGAGT CAGGATGGGA GGAAGCAAGG 240
AGGAGTGGTT TACAGAAAGT ATTTCTGTGT AAGGGATACC ACAGTTGGAA GTTCCCTCTG 300
GATACCCATG GGACTTGAAC TCACGCTGCA TCAGGGCTTC CTGAGCTCCT CAGGGACATC 360
AGGTCACCAA CTCCTTGTTT AGGATGGACT CTCCCTGTGG GGACAGGGAA GGAACTGGAG 420
CTGAAGTAGA TGTGAGAGGT GAAGGTGGCA GACTGTTGGG GCTCTGGAGA ATCTTCCAGA 480
CATTCCTGCT GCCTCTCCCA GCAGACTATG CCAATGAATG AATCAGAAAG CTTGAAGAGG 540
GAAGCAAAAG ATGAAAGAAA TCCTGGGACC ACGCAGCTTC AGAGGGCTGG ATGCCACAGT 600
CCCCAGGCTC GGGAATGAAC GCCTTAGCTG GAGCTTGGGG GCTTGGTGTC CCTGGACTAC 660
CCACACCGTA GCTCCAGGCA GGTTGCTATG CATGCTCACG TCATCATCCA TATTCAGTTT 720
CATCAATTAC ACTCAGTAAT ATCCTTGACA ACTATTTTTT TCCTCAATTC AGGATTTAAT 780
CCAGGATCAC ACATTGCATT TGGTTGTTAT TGTCTCTTCA GTTTCTTTTA AATTGGGCAA 840
ATCCTTAACC TTCTTTGTGT TTTATGACCT TGACTTTTTT TGTGTGTGGC AAAAAAGTTC 900
AAATTATACC TTGACATTTT AAAATAGTAC AGGTCAATTA TTAAGTAACA TTTCTTGTGA 960
TTAAATTCAG 970
|
