| Tag | Content |
|---|
EnhancerAtlas ID | HS098-59065 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:136113630-136114810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:136114640-136114659 | TTACCAGCTGGGGGCGCTG | + | 6.21 | | KLF14 | MA0740.1 | chr9:136114045-136114059 | GAGTGGGCGTGGTC | - | 6.65 | | Klf12 | MA0742.1 | chr9:136114044-136114059 | AGAGTGGGCGTGGTC | - | 6.51 | | SP3 | MA0746.2 | chr9:136114046-136114059 | AGTGGGCGTGGTC | - | 6.32 | | SP4 | MA0685.1 | chr9:136114044-136114061 | AGAGTGGGCGTGGTCGG | - | 6.07 | | SP8 | MA0747.1 | chr9:136114046-136114058 | AGTGGGCGTGGT | - | 6.74 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_24494 | chr9:136113585-136114811 | Colon_Crypt_2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I133236 | chr9 | 136111997 | 136115294 |
|
Enhancer Sequence | AGGGAGAGAG ATGAGAGAAA GGCCCCCAGA GCTGGGCAGG GTTGGGGGAA GAACCGTGGG 60
CAGTGGGAGC AGCGACCCCA AATTCAGCCC CGGGCCCCGC CTCCAGGCCA GCTCCTGGCA 120
GGGTGGCCCC ACCAGGGTGA AGGGCGGCTG TCCGCGGCCT CCAGGTCACC AGCAGGGCCT 180
GGCTTATGAT CTATGAACCC CCGGCCGATC TAGAGGTTAG GGCTCTAGAT GGGGCGGGGA 240
TTCGGTTAGA GAGGGCAGGG TGGAGGGGAG GATAGACAGG AACCAGGGAG GTCCAGGCCC 300
AGTGGGGGCT GAGCTGAGCG GGGGAGGCGG GGCCGAGAAG GGCGGGGCAG AGGAGTGGGA 360
TGAGCGTGGT TGGGGCAGGG CCAGTGGGGC AGGGTCAAGG CTGTGTTGAG GGGTAGAGTG 420
GGCGTGGTCG GAGCGGAGCC GGTGGGCGGG ACCCGGCGGT GTGGAGCTGC ACCCGGAGTT 480
TGTAAGGATC AGGAAAGCTG CCTGGAGCTG GGCAGACAGG CTGACCCAGG GACCCTGACC 540
ACCTACCTGA GCTTCCACCC AGCTTCAAGG CTGTGGGGAT CGTTTCTTAG CCAAGGTGAA 600
AGGCCCTGAG CCCTCCAGTG GGCTCTGAGG GTTTGAATGT TTATTCTAAA TGGGCTCCAA 660
CACGGAGTGC GCGTGCGCTC AAGGACCAGC TGGCTAGGAG CGCCTTCTCT CCCCGAGGGG 720
ATCTGGAATG TTCATCCGCG GTCTTCCCAG TGGTCCTCTC CTGAGCACCC TGGGCATGGG 780
GTTGGGAAGT GGGCACACTT CTTCAGTGCG TGGTACTTTC TGTCCCTCCC AATGACATTG 840
GTCTCTTCCA AATTCCCCAG GCATAGGAAC AGCCACAAGA GCCAACTCAC ATTTCCCAAA 900
GCCCTCTGGG GGCACGGCAG CGCCCTGGGC AGAGGAGAGA ACTGCCCAGC TCAGCGGGGA 960
GAAATCCCAG TGGTGCTTTC CGTTCCCCCC AGGCTCGATG ACTGCCATAC TTACCAGCTG 1020
GGGGCGCTGG TGAGCACTGC CAGTCTCCAG CGCCCGCCCT TACCCCGGGG CAGTGCTGCT 1080
TACAGCACGG CGACTCCTAA AGGCAAGGAG TTAAAGGCAC ACGGATCCTA GCACTTTGGG 1140
GAGGCTGAGG TGGGCGGATC ACTTGAGGTC AGGAGTTCGA 1180
|
