| Tag | Content |
|---|
EnhancerAtlas ID | HS069-00079 | Organism | Homo sapiens | Tissue/cell | GM18951 | Coordinate | chr1:16405130-16406510 | 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: 3 | Chromosome | Start | End |
| chr1 | 16405357 | 16406103 | | chr1 | 16406117 | 16406245 | | chr1 | 16405559 | 16406435 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I016078 | chr1 | 16404981 | 16406456 |
| Enhancer Sequence | CTCTACTAAA GATACAAAAA AAAAAAAAAA AAAAAAAAAA AAAAGCCAGC GTGGTGACAT 60
GCACCTGTAA TCCCAGCTAC TCTGGGGGCT GAGACAAGAG AATCGCTTGA ACCCAGGAGG 120
CGGAGGTTGC AGTGAGCCAA GATCACGCCA CTGCACTCCA GCCTGGGTGA CAGAGAGGGA 180
CTCTGTCTCA AAAAAAAAAA AAAAAAAAAA AAAAAGAGGC GCCCTGAGTT CATCTCTAAA 240
ATGCCCGGCC CTGTCCTGGC CCATGGTGGC TGCTATGTGA CAGGGTCCCT TCCTCAAGGT 300
TCAGAGGGCT GGTACTCCAA TTCCTAGATC TCAGGATCTC TGCAGGTAGA AGGAAGCCCC 360
CCTGCTAGAA CTGTTGCTTT TCCAGAGCTG TGAGTGTGAG GCAGCCGCTG GCCATCAGGG 420
GGCAGCCTGA GACAGCATCA TTCTCTGTTG CTTTCCTTTT CCTTCCTCCC GCCGTCTGCT 480
GACCCAGAAA GTACCCTGCT GGTAACTCAG CCCCAGCCAT GGCTCTGGGT GGTGCATGCT 540
GCACCCTGCA CAGAGGAGCC TGGCTGAGTG GGAGGGGACC AAAACCTGCC CGTGCTCTGG 600
TCCCAAAGCC CTGAGCTCTA CCGTTGTGTA GAGCTCTGTG TCTGCCCCAG GACAGGGAGG 660
TTTTTTCCTA GCACAAAGGT GTCACTTCCT CTAAGCTGTG CACTCACAGG GTGCATCTAC 720
CCAGAGGGAA GGCCTTTTAC AATTTTGCAC AAAGTCTCTG TATAGCCTAG CCAGGCTCCT 780
GAAGTCAGAC AACACGTGGT CCTGACCCCC ATTGTACAGA TGCGGAGACT GAACCCCAGG 840
AAAGGAACCA AGGCCAGTTA GGAGCACAGC TGGGACTGGA ACACCACAGC CAGCAGGACC 900
CGCTGCTCCA GTCTGGAGGA GTCAGGTGCT AGGTGTCACT TCTGGTGTCC TGGCCCCGCC 960
TGGGGTTTCC CCGGGGCTAG GACTTGGGGC CTTTCTGGGG AGCCTGAGAA AGTCACAGGC 1020
CGTTCTCGGA ATATGCCTAC TCTCACTTCC AGGCTCCGAC TGGAATTGGA TGTTAGGTCA 1080
GAGCCCTCCC CAGGAAAGCA GGCTGGACTA GGTGGGATAG GCCGAGACAG AAAGTTGAGC 1140
CCCTAGTCTG ATGGGGGAGA CAGAGCCCTT AGGGAATTCC AAGTCTGATG CAGGAGACAC 1200
AGCCATGCTG CCAGGCCCTG TCCTGAGCAC TGGGAACACG GATGAATCCA GTCCCTGTGC 1260
CGGGGAAGCT CCTAGCCTGG TGAGTAAACA GGTGTTTACT CCCAGCCCCA GTGCGGCGAG 1320
AGCCCTGCTG ACCAGGTCAA GCCATTAGTG GGAGCTTGAG GGGCAGTTTC AGGTGTCTGG 1380
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