| Tag | Content |
|---|
EnhancerAtlas ID | HS191-03817 | Organism | Homo sapiens | Tissue/cell | Trophoblast | Coordinate | chr1:236291760-236293040 | 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 | ATCTGTCACC AATAATGTAA GAACAGCCCA AGGTCTTCTG TCACCACCGT TAAACTGTCA 60
GGATCAGCAC CATTCGTGGC TCCCAATTGG TGGGCTCTCA TGTTCTAGAT GTAGGGCTAG 120
GCACTTACAT GCATTATTTT ATTTCATTTT CGCAGTAGCT CTGTGAGGTT GATGGCCTAG 180
TCTGGACAGG AAGAGCGGTG GGTACTGACA AGGCTGTGCT TACAGTACAT CAGTGAAGCA 240
CAGCACTTGT GCATCCCAGC AAAGCTCAGA GCGACCCATT TCTCACCTCA GTAGCTGGCA 300
TCCGCCTGCC AGTGGCCTGC CTCATTCTCT GGGGTCCCAG CCCGCTCCAG AAACTCACCC 360
AGCTCGCTGA CAGGGGACTG TGCAGGCTGC TGCTGTAACC TGGTGGTGGG CTGTCATCAG 420
ACGGCCATAG AGGATCGCCC TGAGGCTTGG TTGTGGAGGT TGTCAAAGCA GAAGGCTGGC 480
AATATTCCCA TGGCCCAGAA CGTGCTGAGG CAGCATATGT GAGTCAGGCC ATGGCTGCTG 540
CAGCCACAGT GGGGCTTTGT GCTGTGATCG TGTGCAGAGC AGAGCAGCCA CTCAGCCATC 600
CACTGACTCT CCAAATTGCT TCTGAGCACC TATAATTCCA GTTCTCCTGG GAAAAGCCCT 660
GCAAGACCCG GGCTTTCCCC TACCCTGTTC TGCTGATTCC TTTTGGTTGA TTTCCCAGTA 720
TGAGATCCAG CATTATTCCT TTTGAAATTG CAATCCCTGC TGTTTTCCCA CATTGAGAGC 780
ACAACTAAGA AGCACTTTCT TAAGAATCTG CTTCCAGGTG CTCTTGGACC AAGTTTAAGT 840
TCTCTGTCTA CTCTAGTAGG GTCCGTCTAT TCCCAGGGCA TCTGTCTGAA GCGGGGCCTC 900
TGCTGGCCAA ATCCTACTAG CCAAGACCTG GATCTCCCAG AGCTCAGAAA GCTCCCACTA 960
GCAGGGCCCC TTGGCTTGCC TTCCTGCCTC CTTTCTCTCC CTTTGTCCCC TAGTGTCCAG 1020
ATGAGAAGAC ACAGGATGGC TCTCGTCCCA AGAAGGCCTT CGCTTGTGCT GTGGGCACAG 1080
AGGTCTTTCT CCCCTCTCTG AGCACAAAGC AGTCACTGTG CTCTGCCGAG CAGAGGAAAA 1140
ATGCAAATGG TGCTCTGGGT GTGGCCAAGT TCCTTGGGCC CCAAGTGCTG GCCTGCATTC 1200
TTTATGGGGT AGCCTTTGTT TTCCCTTTCT GCAGGCTGTG CCTGAAATAT GAAGATTACT 1260
TAAAACTCAT ACTATGCCAG 1280
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