| Tag | Content |
|---|
EnhancerAtlas ID | HS170-00586 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr11:45053530-45054380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr11:45053916-45053934 | TGGCCACACCCCCTTTTG | + | 6.3 | | TBX20 | MA0689.1 | chr11:45053962-45053973 | CTTCACACCTT | - | 6.32 | | TBX21 | MA0690.1 | chr11:45053963-45053973 | TTCACACCTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_33426 | chr11:45042089-45053722 | H2171 | | SE_33426 | chr11:45053828-45060538 | H2171 | | SE_66866 | chr11:45042089-45053722 | H2171 | | SE_66866 | chr11:45053828-45060538 | H2171 |
|
| | 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 |
| GH11I045032 | chr11 | 45053829 | 45060538 |
|
Enhancer Sequence | AATTCAGAGA CATGTCCCGG GTGGGCATAG AAGGCCCACG ACCATCAAGG ACCCAGGCTC 60
CTTCCATCTA GCTGCTTCAC TACCCTTAAT ATCAGCCTCC TAACTCATGG TTCACTGTGG 120
CTGCTTGAGC TCCAACCATT ATGTCTGCAT TCCAGCCATG AGAAAGAAGA GTACTTCCAC 180
TGTATGTAAA ACTACATCTT GAAAGTTGCA CATGTCATTT TTGTTTGTAC TCCTATGTTC 240
ACAGCTTAGA CACATGGCTA TACCTAGCTG CAAGAAAGGC CAGGAAATGT AATCTTTATT 300
CTGAGTGGCT ACATTCTCAG CAGAAAAAGT GGAAATCTGA GATCAGGTAA AAAAGGGGAA 360
CTGAGAGTTG GGGCAACTGG CAGGCTTGGC CACACCCCCT TTTGCTATAG TTCATTTGAA 420
CTTGCATGTC AGCTTCACAC CTTTGTTGAG AATATGTGGT GGCCTCTTCC TACATTTCTG 480
GGACCTTTTC TCCACTCTTG CCTTCATTCA TTGTGCTTTG GGCACCCCAC ACTCCTCTGG 540
CCTTGGGGGC CTCCCACACA CTGTGCCTCT GCTGGCAGTG ACTCCCTGAG AGCCACCTAT 600
CCTGGATGCA ATGCCTCCCA CTCATCCTCC GGTCTTCAGA TGAAATGACA GCTCCCCAGA 660
GAATCTTCCC ATATCCCAAA GGGTCAGGGT CTGTTAGATG GTCTCACAGC CTTCTGACCC 720
TCTTTGTTAC AGCATCCATT GCAATTGTAA TTGGTGATTG AGTTGTGTGA TCAGTTGTTC 780
ACTCACTGTC TCTCTTGCTA GACTATGAGC TCTTGAGGAT GGGGCCACCT CTGTCATGTG 840
CATCCACCTG 850
|
