| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00005 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr1:1617500-1618380 |
Target genes | | Number: 26 | Name | Ensembl ID |
|
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: 5 | 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_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 | TGGCACGATC TTGGCTCACC ACAACCTTCG CCTCCCAGGT TCAAGCGATT CTCCTGCCTC 60
AGCCTCCCGG GTAGTGGGGA TTACATGCAC GTGCCACCAA ACCCTGCTGA TTTTGTATTT 120
TTAGTAGAGA CGGGTTTTCA CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCTCGTGA 180
TCTGCCTGCC TCGGCCTCCC AAAGTGCTGG GATTTACAGG CATCAGCCAC TGCGCCCAGC 240
CTCCCTTTTC TTTTTTTTTC TTTTTTTTTT TTTTTTTTGC TGACTCATGG GTTAGAATTC 300
CGGATTGGGC AAATACATAA ATATTTTGTA CATGACGGGA GGCAGATTTC ATCATGTGAG 360
TGAAGCGAGA TGCAAACACG AAAGGAAGTC CTTCAGGGCA GTCTTGTAGT GAAAAAATAA 420
AAATAAAAAT GAAAAAAAGA GGCTGGGCAC GGTGACTCAC GCCTGTGATC CCAGCACTTT 480
GGGAGGCCGA GGCGGGTGGA TCACCTGAGG TCAGGAGTTC ATGGTGAAAC CCCATCCCTA 540
GTAAAAATAC AAAAGTTAGC TGGGTGCAGT GGCATGCGCC TGTAATCCCA GCTACTCGGG 600
AGGCTGAGGC AGAAGAATCA CTTGAACCTA GAAGACGGAG GTCGCAGTGA GCCGAGATCA 660
TGCCACCACA CTCCAGCCTG GGCGACAGAG ACTCTGTCTC AAAAAAATAA AAAGGCCAGG 720
CACGGAGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGTC CAAGGGGGTC GGATCATGAG 780
GTCAGGAGAT CGAGATCATC CTGGCTAGCA CTGTGAAACC TTGTCTCTAC TAAAAATACA 840
AAAAATTAGC CGGGCGTGGT GACGGGCACC TGTACTCCCA 880
|
