Tag | Content |
---|
EnhancerAtlas ID | HS133-04989 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:118453720-118454770 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr10:118454040-118454061 | GTTCCCTCCACCTCCTCCCTC | - | 6.16 | ZNF263 | MA0528.1 | chr10:118454044-118454065 | CCTCCACCTCCTCCCTCCCCT | - | 6.18 |
|
| 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 |
GH10I116694 | chr10 | 118453631 | 118454697 |
|
Enhancer Sequence | CACGGGCTTT CCTTCATGAC CCACTGGGTG GCTTCATTTC TGTGACTCTT GGACGTCCCA 60 CTTGAGTAGG TATCCTGCCT TTGCTTATTC CAGCCAAGCA AGCCATAACC CCCTCCCTCC 120 AACTCCAGCC AGCCCCTGGC AAGGTCTAGC TCCTCCTATA CATCAAACAG CTTTTTCTCC 180 TGGAATTTAT TCACGGCATA TTCCCTGCTG GGAGGAGCTA CCTTTGAAAG AAAGGTGCCA 240 GCAAGTTCCC TGGAGTCTCT CTGGCTGAGC TGAGGAATTC ACAAACAACC ACCCACATGG 300 CCACTTGACC TTCTGGGGCC GTTCCCTCCA CCTCCTCCCT CCCCTTCTGA GATGGGCTGC 360 TCACTCCTTT CCTGTTGGCA AATTTGAAAC GCACCAACAT CCTGGGCTTT CTGAGTCCTA 420 AATTTTGCCC CCGAGCCCCT ACGGCTCCTC CTCCTAACTC AGGAGCCCCT GTGCGCTCTG 480 CACTCTCTGC TCCTTCACCT GCCTCGGTGC CCACAGACAC ATCCTCACGT GGCCTCCTGG 540 GCCACCAGGC GCTGAGCCTG TCCCTCTGCA ACCTTTGCTC TTCCAGCAGA CCTGGGTCCA 600 CCTCGTTGTG CCCCTCCCCT TCTGCCCTTT TGCCGCCTGG AACAAAGGGG CTGACCCCTT 660 CTCCAGTTCC AAGCAGGCTT CACAACGCTT GTCTCTGACT GTGGTCACCT TCCCGAACAC 720 CACCCAGTCC CCTCCCTTCC CTCTCCCATG CCTCAACCCC CACCCCACAG TGACCTTGCT 780 GCCAGGCCTC CCCTGTCCCC TTGTCCCCTT ACTGGTGGAA TACTGTTTGC CCAGAACCCA 840 CTCCTTCCCA GCCCACGGGC CCTCTTTCTT CTTGGTTGTC AGATCCTCCT TCTTGCTCCC 900 CAAATGACCC TGTGGCTCTC AGTCTCAGAG CCTCCCTCTC TCCCTGCAGA CAAACCTGCA 960 GAATCTGAGT CAACTGCCTC CACACCACCG ACCTCCACCC TGCAGGCTCT CGGGATTACT 1020 GGGGTCTCTC ACTCTATGCT GTGTTCTGAA 1050
|