| Tag | Content |
|---|
EnhancerAtlas ID | HS138-42166 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr8:134121470-134122600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ETV6 | MA0645.1 | chr8:134122436-134122446 | CACTTCCGCT | - | 6.02 | | MAFK | MA0496.2 | chr8:134121528-134121547 | ACCTGCTGAGTCAGAATCT | + | 6.02 |
|
| | 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 |
| GH08I133110 | chr8 | 134122288 | 134122488 |
|
Enhancer Sequence | ACGGCATCAG CATCACCTGG GAGCTTGTTA AAATGCACGT TCCTGGGCTC CACTCTGGAC 60
CTGCTGAGTC AGAATCTGTA TTTTATCAAG ATTTCAGTCT ACTTTAACGC TTATTGGATT 120
AAAAAGCATG TGTCTAGTTC AATAGCTGTT ATCCAGGCAA ACTAGGGAAA GGTGTTTAGG 180
CAGGAGGAAC AGCAGGCGCA AAGGCTTAAA AGTACGAGAG AACATTTGGT GTTGAGGAAA 240
CAGCACTCCT CACGTGGCCT GGGCATTTTG GTAATATTTC AGCAGCCTAG TTCTCAGGAG 300
TCACAGAAAT TGAAGGCCAA GTGGCAGCTC GTCTGGGTGG CAAGGGCAAA GCACAGCTGG 360
GTTTGTTCCC CACCTGTGTG ACTTACTCAG CTGTGTAAGA CAGCACTTAG CCTCTCTGAG 420
CCAGTTTCCT TGTCCACCCC CTCAGGATGG TTATGGGAGC AAATGAGAAG AGGGTGCACC 480
AGGGACCCAG CACAGCATCT GACACGCAAT GGGTGCTTGG TGCGTGGCAC TTGTGCTGAC 540
CTCGGCTACT CCCTTTGCCG ACATGACTCA GGCAGCATCA TTCTCACCCC TTGGCAGTCT 600
CCTCTAAGTT CCAGCAAATG GCATTGCACA GGGAGGAGAC AGTTTATGAA CTTGTTTTAC 660
TCCTCTGCAG CCCAGGAGGC ATTGGTATCT TGGCTAGGGC TCTCACTATG ACCCCCTCAT 720
GTTATGTATG AGAAAATGGT GCCCAGAGAG AGAAAGCCAC TCTCTCAAGT TTGTACAGTG 780
ATTGCCAGAT AGCGGGTGCT GGGACTTGGA GATCCTGGTG CCCAGACCTC AGTATAGCTC 840
CCTCATGTTA AGATTTGAAG GCAGATTATG CCTGCCACGT AGCAAAGCAG CCTGGGGAGA 900
ACCCACTTTA GTGCCACTGC ACCGTTGTCC TTGTACCCTC CTGGGCTCCC AGAACTGAGT 960
TCTCCCCACT TCCGCTCCAG CCCGGGGCAT TAGACCCACC CAATATCTGA GGTGGGGGCA 1020
TCATGGATTC CTTCTTTATA AAGCATCTGT GAGCAGTACT TGGCCCTCGA ATTTGGCACC 1080
TTCTGCCTTC CCCACCTGCC TTCACTCATC GCCCAATCTC CTTGTTCACA 1130
|
