Tag | Content |
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EnhancerAtlas ID | HS191-24857 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr22:39784290-39785160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF13 | MA0657.1 | chr22:39784326-39784344 | AGCAAGTGGGCGTGGCCT | - | 6.37 | KLF14 | MA0740.1 | chr22:39784329-39784343 | AAGTGGGCGTGGCC | - | 8.12 | Klf12 | MA0742.1 | chr22:39784328-39784343 | CAAGTGGGCGTGGCC | - | 6.48 | SP1 | MA0079.4 | chr22:39784330-39784345 | AGTGGGCGTGGCCTG | - | 7.61 | SP3 | MA0746.2 | chr22:39784330-39784343 | AGTGGGCGTGGCC | - | 6.92 | SP4 | MA0685.1 | chr22:39784328-39784345 | CAAGTGGGCGTGGCCTG | - | 7.76 | SP8 | MA0747.1 | chr22:39784330-39784342 | AGTGGGCGTGGC | - | 7.22 |
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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 |
GH22I039388 | chr22 | 39784006 | 39785732 |
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Enhancer Sequence | CCAGAAAAGG CTCTGGAGCC CAGGCCGGGT GGGAGGAGCA AGTGGGCGTG GCCTGGGCAT 60 GGCCCGTCGG TCAAGGTACT GGCCCTGCCC ACGCCCGGGA GAGGGGCGGG CGAGAGAGAT 120 GCTAAGCCAA TCGGATTGCG GTCATCGGGG GCGAGCGGAG TCTGCAAGAG GTCCGAGGAG 180 TAGCGGGTGC CGAGGGAAGG AGCGCGGCGG GGCGGGTGAG GGATCCCGGG GCTCCGTTCC 240 AGGACACCCA GGTTCTGACC CCGTTTAGGA GTGCGGAGGG CAGGGGCTGC CTGCAACCCA 300 AGGAGCCCGA GCTACCCTGA AGGCCGACCC TGAGGCCGCT GCTCAGCGAG AGGAGCCGAC 360 CCTTGGGGGA CAGCGGGGTC GGGTTCCAAG CCGGGGCTGC TGGGGCTGGT CAGGCCGCCC 420 GCCCTGCTTG ACCCCTCTCA CCTGATGGCT CCCTTCTCCA ATCTTCAAGA AGGTGAAACG 480 TCACTGTGGT CCGCAGAGGG CAGGCCGCGT GTGCGGAGTC GCTGTCATCC CTTAGTGGCC 540 ACGCCCGCCT CCCTGTCCAC TTCCCGTCTT CGTCGTTGCG GTTCAGGTGT TCGCTCCACT 600 CTGCGGCACC AAAGGCCCGT CACGTGCTTC CCCTGCCCAG ACACCCCAAA CACCGAAACT 660 GTCATCCGAA GGCCCCGCAC CTGCCGCCTG TCGGATGCTG AAGAACGAAT CCCAGGTGGA 720 GAGGACAGCA CCCCAAAAGG GATGGGGGAT GGATTGGGGC GTCTGAGCCC CGTGGAGTAT 780 GTCAGCCTTT CAGAGCGACC CGCTCCACGC TGCGATGTGG TCCTTAAGAA GTTAGGGCCG 840 GGCACGGCGC CTCACGCTGT AATCCCAGCA 870
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