Tag | Content |
---|
EnhancerAtlas ID | HS076-03984 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:155016180-155017660 |
Target genes | Number: 36 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:155017560-155017579 | TCTCCACAAGAGGGCACTC | + | 6.44 | EWSR1-FLI1 | MA0149.1 | chr1:155017431-155017449 | GGAAGGAAGGAGGCACAG | + | 6.04 | EWSR1-FLI1 | MA0149.1 | chr1:155017427-155017445 | GGAGGGAAGGAAGGAGGC | + | 7.41 | IRF1 | MA0050.2 | chr1:155016334-155016355 | TTTTGCTTTCATTTTCTCCTG | + | 6.96 | IRF2 | MA0051.1 | chr1:155016333-155016351 | ATTTTGCTTTCATTTTCT | - | 6.01 |
|
| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27386 | chr1:155016985-155017672 | Esophagus | SE_41765 | chr1:155016299-155016775 | LNCaP | SE_41765 | chr1:155016859-155017626 | LNCaP | SE_50747 | chr1:155015129-155018108 | Sigmoid_Colon |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 155016228 | 155016595 | chr1 | 155017065 | 155017634 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I155042 | chr1 | 155015098 | 155018110 |
|
Enhancer Sequence | TGCCTTAAAA GGCCAACCGT CTTCATTCAT CCACCTCCTT CCAGCCTTTA TCCCAATACT 60 GATTTTTTTT TTTTACGTTT AGCTTTGACT TTTGATTTTT TCTTGCCCTT CATATTCCCC 120 TTGGCTCTGA CTTTGTGCCA TTTTTATCTT TCCATTTTGC TTTCATTTTC TCCTGCCTGC 180 TGCGTTGGCA GCGACTTTCC CTCCATTTAG AACAAAGTCC TCAACCCCAC CCAGCCCAGT 240 GTCCAGCTGG GCTGCCCCGG GCCTTGCTCT GCTCTAGCTC CCCTGCTGGT CTCTGGACCC 300 TCTATTTCCC ATCTCCACTC CCAAACACCT GAGATGGGCA GGGCTTGGGT GAGGGCTGCC 360 ACAGGGCTGT TGCTCTGTCT GCCCCTATGT GGGGGGCCTA GAGTGACTGC AAGTGAGTGG 420 GTATGTGTGT ATCTAGGGCC CCATGGGAAG ACAAAGATGA AGGAGCTCTA TTCCTGCCCC 480 CAATAAGCTC ATGATCGCCA GGCATGGCGG CTCACTCCTG TAATCCCAAC ATTTTGGGAA 540 GCCGAGGTGG GAGGATGGCT TGAGTTGAGG TGTTTGAGAC CAGCCTGGGT AACACAGTGA 600 GACCTCGTCT CTACAAAAAA TGAACAAAAT CAGCCAGGTG TGGGGCACAT GCCTGTAGTC 660 CCAGCTACTT GGGAGGCTGA GGCAGGAGAA TCACTGGGAG GTCGAAGCTG CAGTGAGCTG 720 TGATTGTGCC ACTGCATTCT GCATTCCAGC CTGGTGTCAG AGTGAGAGCT TGTCTCAAAA 780 AAAAAAAAAA AAAAAAAAAG CTAATGATCT AGTTGGGATC ATGAGACACC CACAAGACAG 840 AGATGGTTCA AGGGCCATTC TATGGATTGG CTTTTGAGAC GTGTATGGGA GCTGGGAAGG 900 TGCCCCTTGG AAGGGCAATA ACTGGGCTCC AAATGGCCGC AGATGCGGAA CGGTGGTCAA 960 GGAAAGAAGG GTGTCCCTTG CGTAAGGCTC CTGGTATCCA TGGGATGCAG AGGGCAGAGG 1020 CTGGCCTGGA GAACTGAAGT GGGCATGACC AGAACAGTCT GGAAAGCCCT GCAGGAAGAC 1080 CTGGAACTGG CGGTGGTGGC AAGATGGCCT CAGGAAGTCT GGAGGGAGGG CGGGAGGCCA 1140 GGCTGGGTTG GAGGTTAGGG AGCCTGGCCC GGGTAGAGCA TGGCAGGAAG ATGGCTTGAG 1200 ATGGTGGGGG AAGGGGAAAG GTGCAGCGAG GCTCAGAGCC AGCTTGTGGA GGGAAGGAAG 1260 GAGGCACAGA GTCAAAAGCT ACTTCCAGGC TTTCAAGCTG GGTGAGGTCA TGCACTGAAA 1320 GGACAGCTGG CGGGAGGGCA GGCCCTGGCT CAGGAAGCCC AGGCACCACC TCTGTGAGCC 1380 TCTCCACAAG AGGGCACTCA CAGTATGTCT TTGCACTTAC AGTAGTTTTA AAGGCAAAGA 1440 TGTGGATTTT TACAGGGCCC CAGAAGCAAT AGCATTGAAA 1480
|