| Tag | Content |
|---|
EnhancerAtlas ID | HS059-00467 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr1:16405240-16406330 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:16405538-16405557 | TGGCCATCAGGGGGCAGCC | + | 6.46 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 16405357 | 16406103 | | chr1 | 16406117 | 16406245 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I016078 | chr1 | 16404981 | 16406456 |
| Enhancer Sequence | ACCCAGGAGG CGGAGGTTGC AGTGAGCCAA GATCACGCCA CTGCACTCCA GCCTGGGTGA 60
CAGAGAGGGA CTCTGTCTCA AAAAAAAAAA AAAAAAAAAA AAAAAGAGGC GCCCTGAGTT 120
CATCTCTAAA ATGCCCGGCC CTGTCCTGGC CCATGGTGGC TGCTATGTGA CAGGGTCCCT 180
TCCTCAAGGT TCAGAGGGCT GGTACTCCAA TTCCTAGATC TCAGGATCTC TGCAGGTAGA 240
AGGAAGCCCC CCTGCTAGAA CTGTTGCTTT TCCAGAGCTG TGAGTGTGAG GCAGCCGCTG 300
GCCATCAGGG GGCAGCCTGA GACAGCATCA TTCTCTGTTG CTTTCCTTTT CCTTCCTCCC 360
GCCGTCTGCT GACCCAGAAA GTACCCTGCT GGTAACTCAG CCCCAGCCAT GGCTCTGGGT 420
GGTGCATGCT GCACCCTGCA CAGAGGAGCC TGGCTGAGTG GGAGGGGACC AAAACCTGCC 480
CGTGCTCTGG TCCCAAAGCC CTGAGCTCTA CCGTTGTGTA GAGCTCTGTG TCTGCCCCAG 540
GACAGGGAGG TTTTTTCCTA GCACAAAGGT GTCACTTCCT CTAAGCTGTG CACTCACAGG 600
GTGCATCTAC CCAGAGGGAA GGCCTTTTAC AATTTTGCAC AAAGTCTCTG TATAGCCTAG 660
CCAGGCTCCT GAAGTCAGAC AACACGTGGT CCTGACCCCC ATTGTACAGA TGCGGAGACT 720
GAACCCCAGG AAAGGAACCA AGGCCAGTTA GGAGCACAGC TGGGACTGGA ACACCACAGC 780
CAGCAGGACC CGCTGCTCCA GTCTGGAGGA GTCAGGTGCT AGGTGTCACT TCTGGTGTCC 840
TGGCCCCGCC TGGGGTTTCC CCGGGGCTAG GACTTGGGGC CTTTCTGGGG AGCCTGAGAA 900
AGTCACAGGC CGTTCTCGGA ATATGCCTAC TCTCACTTCC AGGCTCCGAC TGGAATTGGA 960
TGTTAGGTCA GAGCCCTCCC CAGGAAAGCA GGCTGGACTA GGTGGGATAG GCCGAGACAG 1020
AAAGTTGAGC CCCTAGTCTG ATGGGGGAGA CAGAGCCCTT AGGGAATTCC AAGTCTGATG 1080
CAGGAGACAC 1090
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