| Tag | Content |
|---|
EnhancerAtlas ID | HS017-22104 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr22:39783940-39785130 |
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: 2 | Chromosome | Start | End |
| chr22 | 39784774 | 39784929 | | chr22 | 39784258 | 39784471 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I039388 | chr22 | 39784006 | 39785732 |
|
Enhancer Sequence | CGGGCGTGGT GGTGCATGCC TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATAG 60
CTTGAACCAG GGAGGTGGAG GTTGTGGTGA GCCAAGATGG CGCCATTGCA CTCCAGACTG 120
GGCAACAAGA GCGAAACTCT GTTTCCAAAA AAAAAAAAAA AAAAAAGCAA AAATTAGCCG 180
GGTGTGGTGG TGGGCGCCTG TAGTCCCAGC TACTTGGGAG GCCGAGGCAG AAGAATCGCT 240
TGAACCCAGG AGGAAGAGGT TGCAGTGAGC TGAGATCGCA CAACTACACT CCAGCCTGCG 300
ACAGAGAGAG ACTCTGTCTC AAAAAAAAAA AAAAAAAAAA AAAAATCCCA CCAGAAAAGG 360
CTCTGGAGCC CAGGCCGGGT GGGAGGAGCA AGTGGGCGTG GCCTGGGCAT GGCCCGTCGG 420
TCAAGGTACT GGCCCTGCCC ACGCCCGGGA GAGGGGCGGG CGAGAGAGAT GCTAAGCCAA 480
TCGGATTGCG GTCATCGGGG GCGAGCGGAG TCTGCAAGAG GTCCGAGGAG TAGCGGGTGC 540
CGAGGGAAGG AGCGCGGCGG GGCGGGTGAG GGATCCCGGG GCTCCGTTCC AGGACACCCA 600
GGTTCTGACC CCGTTTAGGA GTGCGGAGGG CAGGGGCTGC CTGCAACCCA AGGAGCCCGA 660
GCTACCCTGA AGGCCGACCC TGAGGCCGCT GCTCAGCGAG AGGAGCCGAC CCTTGGGGGA 720
CAGCGGGGTC GGGTTCCAAG CCGGGGCTGC TGGGGCTGGT CAGGCCGCCC GCCCTGCTTG 780
ACCCCTCTCA CCTGATGGCT CCCTTCTCCA ATCTTCAAGA AGGTGAAACG TCACTGTGGT 840
CCGCAGAGGG CAGGCCGCGT GTGCGGAGTC GCTGTCATCC CTTAGTGGCC ACGCCCGCCT 900
CCCTGTCCAC TTCCCGTCTT CGTCGTTGCG GTTCAGGTGT TCGCTCCACT CTGCGGCACC 960
AAAGGCCCGT CACGTGCTTC CCCTGCCCAG ACACCCCAAA CACCGAAACT GTCATCCGAA 1020
GGCCCCGCAC CTGCCGCCTG TCGGATGCTG AAGAACGAAT CCCAGGTGGA GAGGACAGCA 1080
CCCCAAAAGG GATGGGGGAT GGATTGGGGC GTCTGAGCCC CGTGGAGTAT GTCAGCCTTT 1140
CAGAGCGACC CGCTCCACGC TGCGATGTGG TCCTTAAGAA GTTAGGGCCG 1190
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