| Tag | Content |
|---|
EnhancerAtlas ID | HS002-01273 | Organism | Homo sapiens | Tissue/cell | A375 | Coordinate | chr1:236291840-236293090 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:236292738-236292756 | CCTTCCTGCCTCCTTTCT | - | 6.15 | | Klf1 | MA0493.1 | chr1:236292915-236292926 | TGGGTGTGGCC | - | 6.62 | | MAFF | MA0495.3 | chr1:236292261-236292276 | GTGCTGAGGCAGCAT | - | 6.32 | | MAFF | MA0495.3 | chr1:236292261-236292276 | GTGCTGAGGCAGCAT | + | 6.51 | | MAFG | MA0659.1 | chr1:236292258-236292279 | AACGTGCTGAGGCAGCATATG | - | 6.52 | | MAFG | MA0659.1 | chr1:236292258-236292279 | AACGTGCTGAGGCAGCATATG | + | 6.88 | | MAFK | MA0496.2 | chr1:236292259-236292278 | ACGTGCTGAGGCAGCATAT | + | 6.24 | | Sox3 | MA0514.1 | chr1:236292972-236292982 | CCTTTGTTTT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCCCAATTGG TGGGCTCTCA TGTTCTAGAT GTAGGGCTAG GCACTTACAT GCATTATTTT 60
ATTTCATTTT CGCAGTAGCT CTGTGAGGTT GATGGCCTAG TCTGGACAGG AAGAGCGGTG 120
GGTACTGACA AGGCTGTGCT TACAGTACAT CAGTGAAGCA CAGCACTTGT GCATCCCAGC 180
AAAGCTCAGA GCGACCCATT TCTCACCTCA GTAGCTGGCA TCCGCCTGCC AGTGGCCTGC 240
CTCATTCTCT GGGGTCCCAG CCCGCTCCAG AAACTCACCC AGCTCGCTGA CAGGGGACTG 300
TGCAGGCTGC TGCTGTAACC TGGTGGTGGG CTGTCATCAG ACGGCCATAG AGGATCGCCC 360
TGAGGCTTGG TTGTGGAGGT TGTCAAAGCA GAAGGCTGGC AATATTCCCA TGGCCCAGAA 420
CGTGCTGAGG CAGCATATGT GAGTCAGGCC ATGGCTGCTG CAGCCACAGT GGGGCTTTGT 480
GCTGTGATCG TGTGCAGAGC AGAGCAGCCA CTCAGCCATC CACTGACTCT CCAAATTGCT 540
TCTGAGCACC TATAATTCCA GTTCTCCTGG GAAAAGCCCT GCAAGACCCG GGCTTTCCCC 600
TACCCTGTTC TGCTGATTCC TTTTGGTTGA TTTCCCAGTA TGAGATCCAG CATTATTCCT 660
TTTGAAATTG CAATCCCTGC TGTTTTCCCA CATTGAGAGC ACAACTAAGA AGCACTTTCT 720
TAAGAATCTG CTTCCAGGTG CTCTTGGACC AAGTTTAAGT TCTCTGTCTA CTCTAGTAGG 780
GTCCGTCTAT TCCCAGGGCA TCTGTCTGAA GCGGGGCCTC TGCTGGCCAA ATCCTACTAG 840
CCAAGACCTG GATCTCCCAG AGCTCAGAAA GCTCCCACTA GCAGGGCCCC TTGGCTTGCC 900
TTCCTGCCTC CTTTCTCTCC CTTTGTCCCC TAGTGTCCAG ATGAGAAGAC ACAGGATGGC 960
TCTCGTCCCA AGAAGGCCTT CGCTTGTGCT GTGGGCACAG AGGTCTTTCT CCCCTCTCTG 1020
AGCACAAAGC AGTCACTGTG CTCTGCCGAG CAGAGGAAAA ATGCAAATGG TGCTCTGGGT 1080
GTGGCCAAGT TCCTTGGGCC CCAAGTGCTG GCCTGCATTC TTTATGGGGT AGCCTTTGTT 1140
TTCCCTTTCT GCAGGCTGTG CCTGAAATAT GAAGATTACT TAAAACTCAT ACTATGCCAG 1200
GACACGGACA CCACAATAAA CTGGGTAATG AGTGTCAACT CAAAGACTAT 1250
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