| Tag | Content |
|---|
EnhancerAtlas ID | HS044-05061 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr16:11406370-11407560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr16:11407297-11407308 | TATTGTTTATT | + | 6.62 | | IRF1 | MA0050.2 | chr16:11406673-11406694 | TTTCACTTTCAGTTTCTTGGA | + | 6.04 | | IRF1 | MA0050.2 | chr16:11406667-11406688 | CTCTGGTTTCACTTTCAGTTT | + | 8.97 | | IRF2 | MA0051.1 | chr16:11406666-11406684 | TCTCTGGTTTCACTTTCA | - | 6.24 | | TFAP2A | MA0003.3 | chr16:11407184-11407195 | TGCCTCAGGCA | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_33035 | chr16:11406212-11407358 | H1 | | SE_62053 | chr16:11386770-11424077 | Toledo | | SE_68718 | chr16:11405593-11411409 | H9 |
|
| | 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 |
| GH16I011306 | chr16 | 11400381 | 11411109 |
|
Enhancer Sequence | CAAAAAAATA AATAAATAAA GTTTAGGCCC TGTCTCGCCC AAGGGAGGTT GGCACTAGCA 60
TGACTTGACA AATCAGTGCC ATATAACTGT TGTTCCAGTT GGGACACAGG AAACTTGCCA 120
CCTGCAAGCC CTGGCCCAGT GTAAAGCTCA AGTCCAGAGG GCTGGGGTTT GTGGGAGACA 180
GAACTGTCAC CCCAGGACTA TCAGAGAGAG AGGGGCTCCT GGCTCTTATT TCTGCAGAAG 240
CAGCTAGATG GACAGGTCCC TCACTCCAAG GAGCCTCCAC CACGTGCCCA CACCTTTCTC 300
TGGTTTCACT TTCAGTTTCT TGGAAAGGCT GTCCTTCCCT ACTCCAAGCC CCTCCCCTCA 360
CTCCCCACCC AGGATCTGGG CACTGGAGGC GCCAGACATC TTATGCCCTG TCCAAGGCTA 420
GCAGGTAAGA AACGCCCCTT GTATCTGCCA AGGTCAAAAT CATACACACC CAGGTGGGGC 480
AGTCCCACCT CTGGGAGGTG TCTTGCAGAA GCACTCCTAG GAGTGTGAGG TGATTTGGCT 540
CCACAGTGCT TGTGGTCAGA AACAACTGGA AAGAAGTTGT GTGCTCAGCA GCATGGTGGG 600
GTGAGGGGGT TGCAGGGCAT CCCACGCCAT AACCCACGAG GTAGCCTCTA TGGGCTGATG 660
GGGGATCAGT GCAGGGTGGT AAGGGCCAGG GCCAGGTCTG AAGGGAGAGT GGGCTCCCAT 720
TCATGTGAGT GGGAAAAGCA ATGTATGTGT CCAGGTGCGC CAGGTCGTGC AGAGCATATC 780
TTGAAAAGGC ACACAAGGGA TTGATCAGAG AGGTTGCCTC AGGCAGGATA ACTGAGATCT 840
GGAAATGGTG TGGGAGGGGA ACCAGTTTTT TTTCTGTGAA GTCCTTGGAT GCTTTGAATT 900
TTTGTTTAAG TCATGCGCAT GCATGATTAT TGTTTATTCC CTGCCCCCAC CCCACCTCAA 960
GTACAGAAGA AAAGAAAGAC AGTTTCTTTC TTAAACTAGT TTGCTGGAGG GCTGGACATC 1020
CTTTGTTGCT CATTTTCTGG GAGATGTAGG TTAAAATTAA CCTACATCTT TGGAGGGCTT 1080
TGGAGTCAGA CTGTCTGTGT TCAAGTCCTG GCTGCCCCAC TTTGTAGCTT CTCGAGCAAG 1140
TCGCTTAACT TCTCTGAGCT TTTATTTTCT CTCCTGTAAA ATGGCACAAT 1190
|
