Tag | Content |
---|
EnhancerAtlas ID | HS034-00720 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:27691580-27692740 |
Target genes | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr1:27692118-27692129 | CTTTCCCGCCC | - | 6.32 | KLF16 | MA0741.1 | chr1:27692726-27692737 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:27692099-27692109 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:27692425-27692435 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:27692726-27692736 | GCCCCGCCCC | + | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34417 | chr1:27690765-27694847 | HCT-116 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 27691785 | 27692261 | chr1 | 27691800 | 27692047 |
|
Enhancer Sequence | TAGTGTTGCA GGAGAGGAGT TGGGCTCACT GGGTTGGGAC CCTCAGGCCA CGGTTCAGAG 60 CCTGTGAGCA CCTGGCATGG GGGAAGGGAG GCTGTGGACC AGTTGAGTCT GTTACGGGCC 120 ATTTAGGAGG TGGGAGTTGC GCAAACATAG AAGTCCCCTC CCTTTGGTCT TCAGCACAGG 180 CTCTTGAAAG GGGCTACCAT CAGTGTGCAT AGACAACGCT GTGCCTAAAT GTATGTATGT 240 GTATATCTGT GACATGTATA GCTTACTATG TCTGACTGTA TCTGTGTGTG TGACAGCGTC 300 TGCTAGGGCC TGCATGAGTC AACATGTATG CGATTTGTGT CTGTCGATAA TTGTATCTTT 360 GTGTCCGAGT GGTCGGGTCA GCCTTCATTT TAGGCTACGA TTTCATGGAC ATCCAGGAAG 420 CACAGCTACT GGACTCTAGC ATAAGCAAGT AAGTATGGGG GCCGAGCATC CGGGCTGGCT 480 GGAGGGAGGA GTGACTCGCG GGGGAATAGC CTCCTTCTGG CCCCGCCCCT GAGCCATCCT 540 TTCCCGCCCA CTTCCCCGCC CCTTCCCCGC CCATTCTTTC TGGGCCGCTG AGGCCACTTA 600 ACCTAAGCTC CCTCACCCAG TATCCAGTCC CGTCGGGCCC CTTCGCTTCT CTTTTTGCCT 660 CTCCTAGCCC GATCCTTGGA AATAGTATGC TAGGACTCCT GAACTCCAGC CTCCCGGCCC 720 CTTTCCCTAA GTCCAAGCTC CTCTCCCAGT AATTGTCCTC AAGAGATCCG CGTGACATTC 780 TCCTGAGGGT GAGGCTGAGT TCTCCAACCC CACCCCTGAG ACACCACAGC CCCGCGCCGC 840 TCCCCGCCCC GCCCCAGAGT TCCAAAGCCC CTCCCCATCC TTGCCCCGCT GGCTGGGCAC 900 CGCTCCGACT GAAGGGTGCC TAAGCCCCAA CCTCGAGCCC TAGAGCCGCG CCCGGATCCC 960 TGTCTCGTCC CGAGCCCGGC CGCGCCCCAG ATCCCCTAAA TCCCACTTTT TTCACGGCCC 1020 TGTCCCAAGC CCTTCAGCTT TAGCTCACTT TAAGTCCCCT AGACCCGGTA CCCCTCTCGG 1080 CCCCTCCCTT GAGCCTTCGA GCCCGGCTTG GTCCCCTCCC AGGACCCTGA GTCCCGCCCG 1140 GATCCGGCCC CGCCCCCAGC 1160
|