| Tag | Content |
|---|
EnhancerAtlas ID | HS047-22948 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr22:39784150-39785230 |
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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 39784774 | 39784929 | | chr22 | 39784258 | 39784471 | | chr22 | 39784432 | 39785200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I039388 | chr22 | 39784006 | 39785732 |
|
Enhancer Sequence | TACTTGGGAG GCCGAGGCAG AAGAATCGCT TGAACCCAGG AGGAAGAGGT TGCAGTGAGC 60
TGAGATCGCA CAACTACACT CCAGCCTGCG ACAGAGAGAG ACTCTGTCTC AAAAAAAAAA 120
AAAAAAAAAA AAAAATCCCA CCAGAAAAGG CTCTGGAGCC CAGGCCGGGT GGGAGGAGCA 180
AGTGGGCGTG GCCTGGGCAT GGCCCGTCGG TCAAGGTACT GGCCCTGCCC ACGCCCGGGA 240
GAGGGGCGGG CGAGAGAGAT GCTAAGCCAA TCGGATTGCG GTCATCGGGG GCGAGCGGAG 300
TCTGCAAGAG GTCCGAGGAG TAGCGGGTGC CGAGGGAAGG AGCGCGGCGG GGCGGGTGAG 360
GGATCCCGGG GCTCCGTTCC AGGACACCCA GGTTCTGACC CCGTTTAGGA GTGCGGAGGG 420
CAGGGGCTGC CTGCAACCCA AGGAGCCCGA GCTACCCTGA AGGCCGACCC TGAGGCCGCT 480
GCTCAGCGAG AGGAGCCGAC CCTTGGGGGA CAGCGGGGTC GGGTTCCAAG CCGGGGCTGC 540
TGGGGCTGGT CAGGCCGCCC GCCCTGCTTG ACCCCTCTCA CCTGATGGCT CCCTTCTCCA 600
ATCTTCAAGA AGGTGAAACG TCACTGTGGT CCGCAGAGGG CAGGCCGCGT GTGCGGAGTC 660
GCTGTCATCC CTTAGTGGCC ACGCCCGCCT CCCTGTCCAC TTCCCGTCTT CGTCGTTGCG 720
GTTCAGGTGT TCGCTCCACT CTGCGGCACC AAAGGCCCGT CACGTGCTTC CCCTGCCCAG 780
ACACCCCAAA CACCGAAACT GTCATCCGAA GGCCCCGCAC CTGCCGCCTG TCGGATGCTG 840
AAGAACGAAT CCCAGGTGGA GAGGACAGCA CCCCAAAAGG GATGGGGGAT GGATTGGGGC 900
GTCTGAGCCC CGTGGAGTAT GTCAGCCTTT CAGAGCGACC CGCTCCACGC TGCGATGTGG 960
TCCTTAAGAA GTTAGGGCCG GGCACGGCGC CTCACGCTGT AATCCCAGCA CTTTGGGAGC 1020
CAAGGTGGGC GGATCATCTG AGGTCAGGAG TTCGAGACCA ACCTGGCCAA CATGGTAAAA 1080
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