| Tag | Content |
|---|
EnhancerAtlas ID | HS062-00274 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr1:26689950-26691020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:26690485-26690504 | GGGCGCCCCCTGCTGGGCG | - | 7.06 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 26690259 | 26690771 | | chr1 | 26690789 | 26690930 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I026363 | chr1 | 26690341 | 26690550 |
| Enhancer Sequence | AGACCTGCTG AATCAAAAAC TCTGGGAGGG CTGGGCACAC TCTCGTGGCT GTAATCCCAG 60
CATTTTGGGA GGCCGAGGAG GGAGGATCAA TGGAGCCCAG GAGTTCAATA CCAGCCTGAG 120
AAACACATTG GGACCCCGTA TGCACAAAAA ATTTGAAAGT TAACGAGGAG TGGTGGTGTT 180
TACCCTTCGT CCCAGCTACC GGGGAGGATG AAGTGGGAGA ATCCCTTAAG CCCAGGAGTT 240
TGAGACCAGC GTGGGCGACA GAATGAGACT CCATATGGAA AAAAAAAAAA AAAAAAAAGA 300
TAACTCTGGG GCTGGGAGCT ACTCTGGAGG CTGAGGTGGG AGGATCACAA AAACTCTAGG 360
AATCTGCATG TTTACTAGCT CTCCAGGTGG TCTGAGGCTC ATGAAAGTTT AAGAACTCCT 420
GCCCTGCAGG ATCCAGCAGG GCTTCTCCCC ATAACCACAA TGTGCCTTCA ACTTCAGAAC 480
TAGCCAGAGA GCGCACAGTT TCCGCCCTTT GCTAACGCAC TGAGATGCGC TCCCTGGGCG 540
CCCCCTGCTG GGCGATGCGG ATGGTGAGGC CAATCGCATC GGCGGTCGCG CAGATTTGTG 600
GGATCCCACT TGAAAAAGGT TGGTCATCGG ACTGTGGTCT AGACTCACCA AAATCTACCC 660
ATTCCCTCAT CTGACTGCCC AAAAAAATAA ATAAGAAGCT TAACTTGGAG TCCAGAAAGG 720
ATGGTTGTCC AGGTAAGGGC TTTCTTTGCC CAGAGCAAAT GTTGAGAGAC TAAACCTAAC 780
ACTACCGTTA AATCGGGGTA ATCTTAGGCA AACGCTGCCC ATTAAAAGCC TCAGTCTCCC 840
CATTTTAACC TAAATGAGAC GATCTCATAG GCAGTCCTCT AGGGTGGCGA GGACTTTGGT 900
GGCCGTCTTA TCCGATATCT CCACCCAAAT GAACCATCCA AGGTCACTTG GCCCTAGAGG 960
TTGCCCAGGA GTGCCTTCTA GCTTTGAGGT CCTTGCTTCT AGAAGCAGAC TCGGGTGCAT 1020
GGGGGGCCCT GAAGGATGTT GAGGGGAGAA GCAGAGCCCA GGAGGCAGAT 1070
|
| |
|
|
|
