| Tag | Content |
|---|
EnhancerAtlas ID | HS133-16890 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:47998320-47999250 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr2:47998698-47998715 | AAGTGGGAGGGACTTAC | - | 7.04 | | ZNF263 | MA0528.1 | chr2:47998519-47998540 | TTCCTCTCCCATTCCTCATCC | - | 6.36 |
|
| | 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 |
| GH02I047770 | chr2 | 47997981 | 47999041 |
|
Enhancer Sequence | GTGATCCTCC TTCTTCAGCT TCCCAAAGTG CTGGGATCAC AGGTGTGAGC TACCACACCC 60
AGCTGTCAGG TTTCTTATTT ATGTGTCTCA GCTGCAGGTC AGGCAGATGG CTCTGCTGAT 120
CTTGGTTGGG CTCCTTCACA CATCTGAGGG TCAGCTACTC TGGATGTGCT CTGCTAGGCT 180
GACTCAGATC TCCTCCACAT TCCTCTCCCA TTCCTCATCC TTCCAGCAGA CTAGCTGGTG 240
TGCTCTCATG ACAGTGGCAG GAGGCCAAGA AAAAACAAGC CCAATTGTGT GGGAAGGCAA 300
GAGGAAGCTC CCATGTGCTT TTCAAACCTC TGCTAACATC TTATTGGCCA AAGCAAGTCA 360
CATGGTGAGC CAGAGACAAA GTGGGAGGGA CTTACAAAAT TACAGGAAGA AAGAAGGCTA 420
TTGAATTGGG GGCCATTAAG GCGATGAGCT TGCCATAAGG GCTAAATATA CACAGGCATT 480
GTTCTTGAGT GTTGAGTGTA CAGTGGTAAA CAAGCCTTTA ACACCTGAAG TGCAGTGGAG 540
AAGAGCAATA CATAAATAAC TAAGCAAAAT TAGGAAGTTG ATTCCATGAA CTTGTGGACC 600
AAGTGATTGG TGCACAGATG AGAGTAACAA GTGAGGCTGG GCCGGGTAGC TCACGCCTGT 660
ATTCCCAGCA CTTTGGGAGG CCAAGGCGGT GGATCACATG AGGTCAGGAT TTGCAGACCA 720
GCCTGGCCAA CATGGTGAAA CCCCGTCTCT ACTACAAATA GAAAAATTAG CTGGGCATAG 780
TGGTGGGTGC CTGTAATCCC AGCTACTAGG GAGGCTTAGG CAGGAGAATC ACTTTAACCC 840
AGGAGGCGGA GGTTGCAGTG AGCCAAGATT GTGCCACTGC ACTCCAGCCT GGTCGACAGA 900
GTGAGACTGT GCCTCAAAAA AAAAAAAAAA 930
|
