| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04837 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr12:12693340-12694290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr12:12694063-12694075 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr12:12694063-12694075 | TCTATTTTTAGT | - | 6.32 | | NKX2-3 | MA0672.1 | chr12:12693565-12693575 | TTCAAGTGGT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27729 | chr12:12691562-12693971 | Fetal_Intestine |
|
| | 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 |
| GH12I012538 | chr12 | 12691535 | 12693761 |
|
Enhancer Sequence | AACATCCAAT ACAAGGAACA CTAGGTTAGA AAATGCTCAT TCAGCTATTT CCCTTGTACA 60
GTGGGTCTAA CTTGTGCTTC CTTCACTTAC ACAACAGTTT TTGAACATCT ATACTGTGCA 120
AGGCTTTTTG CTCAAGGAAT CTTTGGAGGA TACAATTTTA AAGCAATTTC ATAAGATATC 180
TATAAGGCTC CGTGAGATCA CATAGCAAGA GTGGGAGAGA AAAATTTCAA GTGGTGACAT 240
CTAGAAGTCA ACAGGAGGAG GTGAGGAGGT GGTCAATCCC ACCTATGTAT TTATTCTGGA 300
CGCTCTCCTA CCCCAACTCC TTAGGGTGCT ACACAATCTC TTTGTATTCA CAAATAACCC 360
CTGGTCAAGA GGTTTGGAGG GAGCGGCGAC ACCACCAGCC AGCAAACTTC TACTAATTCT 420
GGAGGCAACT TCCTGTCAGC TGGTCCCTAA AGGCTGGTTG CTTCCTGCCA GGAGGCCACT 480
TAGCACAGAT TCATCTTTCT TCAGGAGGCA GACAGTTGCT TTTTTTTCTT TTCTTTTCTT 540
TTCTTTTTTT TTTTTTTTTT TTTTTTTGAG CCAGGAGTCT CACTCTGATT GCCCAGGCTG 600
GAGTGCAGTG GTGCTGATCA TGGCTCACTG CAGCCTCAAC CTCCCAGGCT CAGGTGATCC 660
CCCCAGCTCA GCCTCCCGAG TAACTGGGAC TACATGTGCA CACCATCACG CCTGGCTAAT 720
TTCTCTATTT TTAGTAGAGC TGGAGTTTCA CCATGTTGCC CAGACTGGTC TCAAACTCCT 780
GGACTCAAGC AATTGACTCA CCTCAGTCTC CCAAAGTCCT GGGATTATGG GCGTGAGCCA 840
CCGCACCTGG CCACTTGCTG ATTCTCACTG TGGCACTGAT TTTAGAGGGA AAGGCAGAGG 900
GGAAGACAAT TCATCTTCCC TTCAACCCCA GGTACACACA GTCCCCTGCC 950
|
