| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00802 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr2:46717590-46718340 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr2:46717976-46717991 | AATCCAAAAATAGAA | + | 7.64 | | PLAG1 | MA0163.1 | chr2:46718008-46718022 | CCCCCTTGAGCCTC | - | 6.35 | | ZNF263 | MA0528.1 | chr2:46718157-46718178 | GGTGGAGGAGGTGGGGAGGGC | + | 6.03 |
|
| | 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 |
| GH02I046490 | chr2 | 46717233 | 46718477 |
|
Enhancer Sequence | TGCCCTGGCG GTGGATGACG GAGACCCCAG GGTTAAGGGG CTTTTGTGGT GCCTCTCAAA 60
TCTCACCCAG AGAGTGACTA TCCTTGGCCT GTACTCCATC AACAGGAGGG AGGGAGGGAG 120
CAGGCTCTGT GCATTTTGCA GGGGCAGGGA CCGTTGGAGC AGGCCATTGG AGGAAGGAGT 180
CTGGTGGCCC CAGGGCAAGT GGCCCCTGCA TGCCTTCCAG CTCTGGGCGC AGAGTCTGCC 240
TGCAGAGGCG CCTCTTCACA AGCAGGTCAC GCTCTAGGCT TCCAGCTGCT AATCACAGGG 300
GCTCTCCAGC TTGGGTGCAT TTCCTCCCTC TGCTCCTGGC TTCCGCCCCA GTCCCATTCA 360
GCTGATCATT CTCCGCTGGG CTAGAAAATC CAAAAATAGA AGAAAGCTAC ACTTTTTACC 420
CCCTTGAGCC TCTTGTATCA AATGACACAG TCACTTTGCC TCAAACTTTT CATCAAAGCA 480
GCCTTTGTAA GGTCCTGGGG CAGAAAGCAG GCCTTGGAAG ACAGCCACCA GGAAGCCATG 540
CAGAAAGTGC TGAGCAGGGG GACCCTTGGT GGAGGAGGTG GGGAGGGCAG GGTTTCAGGA 600
GCTTCCCTCT GCCCCAGAAA GAGCCAGTGA CAGACACTTG CTACCATGGG GCAGCTCTTC 660
TCTGAGCACC AGCTCTAGCT TCAGGTCTTG GAAGTGCAAG AGCAGCAAAT AGTGTGGCTG 720
CACAGACCAC CCATTGCCAG GGTTCAACAA 750
|
