| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00931 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:26689650-26691020 |
Target genes | | Number: 29 | Name | Ensembl ID |
|
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: 3 | Chromosome | Start | End |
| chr1 | 26689724 | 26689857 | | chr1 | 26690259 | 26690771 | | chr1 | 26690789 | 26690930 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I026363 | chr1 | 26690341 | 26690550 |
|
Enhancer Sequence | TCAGATGCGG GATAAATGCT GCCAACTGCC CAGCACCCCT AGCAGGGCCT GAGGTCCTCT 60
CCAAATCTCT GCCCACTTCT CTCTCCCTCC CCGTCATCTC CCTCAGGGCC CATCATCCCC 120
AGGATACTCT ACTCTTTCTG CTGCCCTGTA GGGGAGATGG CAGTGGTCAG AAGGCCAGGG 180
GTAAGAGGTA CCCCAGGTAT ATTGTGGAAC ACTGCTATTC AAAATGTGGT TCACAGACCA 240
GCAGTGCTGG TATCACACTT TGGGAGCATG TTAGAAATGC AGGTTCTCAA GTCCGGCCCC 300
AGACCTGCTG AATCAAAAAC TCTGGGAGGG CTGGGCACAC TCTCGTGGCT GTAATCCCAG 360
CATTTTGGGA GGCCGAGGAG GGAGGATCAA TGGAGCCCAG GAGTTCAATA CCAGCCTGAG 420
AAACACATTG GGACCCCGTA TGCACAAAAA ATTTGAAAGT TAACGAGGAG TGGTGGTGTT 480
TACCCTTCGT CCCAGCTACC GGGGAGGATG AAGTGGGAGA ATCCCTTAAG CCCAGGAGTT 540
TGAGACCAGC GTGGGCGACA GAATGAGACT CCATATGGAA AAAAAAAAAA AAAAAAAAGA 600
TAACTCTGGG GCTGGGAGCT ACTCTGGAGG CTGAGGTGGG AGGATCACAA AAACTCTAGG 660
AATCTGCATG TTTACTAGCT CTCCAGGTGG TCTGAGGCTC ATGAAAGTTT AAGAACTCCT 720
GCCCTGCAGG ATCCAGCAGG GCTTCTCCCC ATAACCACAA TGTGCCTTCA ACTTCAGAAC 780
TAGCCAGAGA GCGCACAGTT TCCGCCCTTT GCTAACGCAC TGAGATGCGC TCCCTGGGCG 840
CCCCCTGCTG GGCGATGCGG ATGGTGAGGC CAATCGCATC GGCGGTCGCG CAGATTTGTG 900
GGATCCCACT TGAAAAAGGT TGGTCATCGG ACTGTGGTCT AGACTCACCA AAATCTACCC 960
ATTCCCTCAT CTGACTGCCC AAAAAAATAA ATAAGAAGCT TAACTTGGAG TCCAGAAAGG 1020
ATGGTTGTCC AGGTAAGGGC TTTCTTTGCC CAGAGCAAAT GTTGAGAGAC TAAACCTAAC 1080
ACTACCGTTA AATCGGGGTA ATCTTAGGCA AACGCTGCCC ATTAAAAGCC TCAGTCTCCC 1140
CATTTTAACC TAAATGAGAC GATCTCATAG GCAGTCCTCT AGGGTGGCGA GGACTTTGGT 1200
GGCCGTCTTA TCCGATATCT CCACCCAAAT GAACCATCCA AGGTCACTTG GCCCTAGAGG 1260
TTGCCCAGGA GTGCCTTCTA GCTTTGAGGT CCTTGCTTCT AGAAGCAGAC TCGGGTGCAT 1320
GGGGGGCCCT GAAGGATGTT GAGGGGAGAA GCAGAGCCCA GGAGGCAGAT 1370
|
