| Tag | Content |
|---|
EnhancerAtlas ID | HS064-10020 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr22:39784140-39785130 |
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 | TAGTCCCAGC TACTTGGGAG GCCGAGGCAG AAGAATCGCT TGAACCCAGG AGGAAGAGGT 60
TGCAGTGAGC TGAGATCGCA CAACTACACT CCAGCCTGCG ACAGAGAGAG ACTCTGTCTC 120
AAAAAAAAAA AAAAAAAAAA AAAAATCCCA CCAGAAAAGG CTCTGGAGCC CAGGCCGGGT 180
GGGAGGAGCA AGTGGGCGTG GCCTGGGCAT GGCCCGTCGG TCAAGGTACT GGCCCTGCCC 240
ACGCCCGGGA GAGGGGCGGG CGAGAGAGAT GCTAAGCCAA TCGGATTGCG GTCATCGGGG 300
GCGAGCGGAG TCTGCAAGAG GTCCGAGGAG TAGCGGGTGC CGAGGGAAGG AGCGCGGCGG 360
GGCGGGTGAG GGATCCCGGG GCTCCGTTCC AGGACACCCA GGTTCTGACC CCGTTTAGGA 420
GTGCGGAGGG CAGGGGCTGC CTGCAACCCA AGGAGCCCGA GCTACCCTGA AGGCCGACCC 480
TGAGGCCGCT GCTCAGCGAG AGGAGCCGAC CCTTGGGGGA CAGCGGGGTC GGGTTCCAAG 540
CCGGGGCTGC TGGGGCTGGT CAGGCCGCCC GCCCTGCTTG ACCCCTCTCA CCTGATGGCT 600
CCCTTCTCCA ATCTTCAAGA AGGTGAAACG TCACTGTGGT CCGCAGAGGG CAGGCCGCGT 660
GTGCGGAGTC GCTGTCATCC CTTAGTGGCC ACGCCCGCCT CCCTGTCCAC TTCCCGTCTT 720
CGTCGTTGCG GTTCAGGTGT TCGCTCCACT CTGCGGCACC AAAGGCCCGT CACGTGCTTC 780
CCCTGCCCAG ACACCCCAAA CACCGAAACT GTCATCCGAA GGCCCCGCAC CTGCCGCCTG 840
TCGGATGCTG AAGAACGAAT CCCAGGTGGA GAGGACAGCA CCCCAAAAGG GATGGGGGAT 900
GGATTGGGGC GTCTGAGCCC CGTGGAGTAT GTCAGCCTTT CAGAGCGACC CGCTCCACGC 960
TGCGATGTGG TCCTTAAGAA GTTAGGGCCG 990
|
