| Tag | Content |
|---|
EnhancerAtlas ID | HS054-00002 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr1:1617620-1618900 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr1:1617775-1617790 | TTTGCTGACTCATGG | - | 6.4 | | Nr2f6(var.2) | MA0728.1 | chr1:1618006-1618021 | GAGGTCAGGAGTTCA | + | 6.22 | | RARA | MA0729.1 | chr1:1618006-1618024 | GAGGTCAGGAGTTCATGG | + | 6.39 | | Zfx | MA0146.2 | chr1:1617982-1617996 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_13835 | chr1:1616834-1618483 | CD34_Primary_RO01536 | | SE_27558 | chr1:1617423-1618832 | Esophagus | | SE_34455 | chr1:1616569-1618227 | HCT-116 | | SE_34455 | chr1:1618494-1619079 | HCT-116 | | SE_40508 | chr1:1617417-1618219 | K562 | | SE_53355 | chr1:1617565-1618375 | Spleen |
|
| | 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 |
| GH01I001685 | chr1 | 1616659 | 1618918 |
|
Enhancer Sequence | TTAGTAGAGA CGGGTTTTCA CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCTCGTGA 60
TCTGCCTGCC TCGGCCTCCC AAAGTGCTGG GATTTACAGG CATCAGCCAC TGCGCCCAGC 120
CTCCCTTTTC TTTTTTTTTC TTTTTTTTTT TTTTTTTTGC TGACTCATGG GTTAGAATTC 180
CGGATTGGGC AAATACATAA ATATTTTGTA CATGACGGGA GGCAGATTTC ATCATGTGAG 240
TGAAGCGAGA TGCAAACACG AAAGGAAGTC CTTCAGGGCA GTCTTGTAGT GAAAAAATAA 300
AAATAAAAAT GAAAAAAAGA GGCTGGGCAC GGTGACTCAC GCCTGTGATC CCAGCACTTT 360
GGGAGGCCGA GGCGGGTGGA TCACCTGAGG TCAGGAGTTC ATGGTGAAAC CCCATCCCTA 420
GTAAAAATAC AAAAGTTAGC TGGGTGCAGT GGCATGCGCC TGTAATCCCA GCTACTCGGG 480
AGGCTGAGGC AGAAGAATCA CTTGAACCTA GAAGACGGAG GTCGCAGTGA GCCGAGATCA 540
TGCCACCACA CTCCAGCCTG GGCGACAGAG ACTCTGTCTC AAAAAAATAA AAAGGCCAGG 600
CACGGAGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGTC CAAGGGGGTC GGATCATGAG 660
GTCAGGAGAT CGAGATCATC CTGGCTAGCA CTGTGAAACC TTGTCTCTAC TAAAAATACA 720
AAAAATTAGC CGGGCGTGGT GACGGGCACC TGTACTCCCA GCTACTCAGG AGCCTGAGGC 780
AGGAGAAGGG CGAGAACCCA GGAGGCGGAG CTTGCAGTGA GCTGAGATCG TGCCACTGCA 840
CTCCAGCCTG GGCCACAGAG TGAGACTCCG TCTCAAAAAC AAATAAATAA ATAAATAAAA 900
AGAAGAAAGA AGATGGATGG AATGACCCCC GCGGTGTCGG CCTGTGAGGG TGCTGTCGGG 960
CCCGAGCGCA CAGGCTTGAA CGGATGGGCG GACGGGCGAC ACGCACGCAC ACACACACCC 1020
CAACACAGCA CATCTGCCCA GAGACAGTCA CACCTGCACA GCGCGCTCCC AGCGCCCTAA 1080
CCTTGGTTTC TAAATATCAT TCTCCACTAA AGGGGCTGGG CGCAATGGCT CACGCCTGTA 1140
ATCCTAGCAC TTTGGGAGGC TGAGGCAGGC GGATTACCCG AGCTCAGGAG TTCTAGACGA 1200
GCCTGGGCAA TGTGGCGAAA CCCTGTCTCT ACTAAAAATA CAAAAAATTA GTCTCTACTA 1260
AAAAAACAAA AAATTAGGCC 1280
|
