Tag | Content |
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EnhancerAtlas ID | HS047-16754 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:10137800-10138820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:10138559-10138578 | TTGCGCCCTCTGGTGTCCA | - | 6.9 | Foxd3 | MA0041.1 | chr19:10137802-10137814 | AAACAAATAATC | - | 6.07 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I010027 | chr19 | 10137829 | 10138918 |
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Enhancer Sequence | AAAAACAAAT AATCATAGAA ACGGGGGTCT TGCTTTATTG AGCAGGCTGC TTTTGAATTC 60 CTGGGCTCAA GTGATCCTCC CACCTCGGCC TCTCAAAGTG CTGGGATTAC AGACATGAGC 120 CACCACGCCC GGCAGGCATA TACCACTGTT TCTTGCTTGT CTCCACCCAC TAAAATGTCA 180 GCTCCATGGG CAGGGGACTG TTGTCTATTT GCTCTACCCA CATCACCAGC ACCGTGGAAA 240 CCAAAAAATG ACTCAAGGAG TTAACCAAGC TGGCACATCC TGGCAGTACA GTCCACCCTG 300 AGAAGCTCCT GACACCTCCT ACCTGGACAA GACAGGGTAC TTCTCTGACC CTCAGTTTCT 360 TCATCTGTGA AATGGAACTT GCCAGGGAGA AAGTTATATT AAGGGCTGGA ATGTAGTCGG 420 GGTCTAATAA ATTAGAGCCC TTAATAGTTA TGTTGATGGT AGCCTTATTC CTTGGTCTCC 480 TGGGTCCTGC CCGGCCTTCC CTGGGAAGCT CTGAGCTCAA AGCCCTGGAG GAGGGAGTAA 540 AACCAGAGGC TGCATCTCTG CAAGGACACA TCCCTGCAAG TCCACCCCTC CCGCCCGCGC 600 CTTCTCGGTG CAAACTCCCG ATCCCAGGGA GGGGAAGGCG GGCGGAATCT GAGCGGCAGG 660 CGCAGCTGCT CCGGGCGGGC GGCCAAGGTT CCCTCCCTCG AGCACTGGCA TTCCTGAGGG 720 AGGGGCCGAG CGCAGCTGCC CGCCTGGCCG GAGGCTCGCT TGCGCCCTCT GGTGTCCAAG 780 TACGAGAGGC CACGTGGACT TGCGCACCAG CAGCCGGTCT GTTCTAGGCC ACTGTCTGCA 840 GCTCAGGTGG ACCTGGGTGG AGCTAGGTCT ACCCCCTACC TTTCTTGGGC TCCCTTTTCT 900 TATCCGGGTT CACGAACTCA GCTTCCATCA CTAAACTTGC TGTGTGACCC TGAGCAAGAC 960 ACTCAACCTC CCTGTACCAC AGTTTCTTAG CTGTGCAATT TGGGACAGGA TCCTTTACCT 1020
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