| Tag | Content |
|---|
EnhancerAtlas ID | HS133-05933 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:66261100-66262670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF1 | MA0595.1 | chr11:66262178-66262188 | GTGGGGTGAT | - | 6.02 | | Tcf12 | MA0521.1 | chr11:66261876-66261887 | AACAGCTGCTG | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I066492 | chr11 | 66259929 | 66261432 | | GH11I066495 | chr11 | 66262541 | 66262630 |
|
Enhancer Sequence | ACAGGTGAGA AGGCAGTGGC CAGCCCTGGC ACCCCAGCCT ACAGCTCCAC TCCCCACAAC 60
CTGCCCTACC CAGCGGTGAA GCTGCTCCAG CCTCTGCCCT CAGGAGCTAT GGGTTGAGTG 120
GGGAAAATGG CCCCTTAGGC AGAGAAGACC CTGTCTTGCC CTCCCTCAAG ATGTCCCAGG 180
AGCTCAGATG CCTGGATGTA GAGCCTGGGT GTACATCTGG GGCTCAGGGA TGAGCCTGGT 240
GTAGAGCCTG GATGTAGAGC CTGGATGTAG AGGGCCCTTC GGGACAGTTC AGCTGCTGTT 300
CCCCGCACCA GGAGGAATTG TTTGGCTCAG GCTAAGGAAG CACACCCTAA GGGCGTGCTT 360
AGGGCGTGGC TCCAGCAGCC CCAGGACAGA CACTTGGGGC AGGGGGCATC TCTGGGTGCT 420
CCCATCTGAG GCAGCAGTGC TGTCTTTGTT TGCGCTGCTG TTCCGTGGAA CCTGGGCTTT 480
TCCGGGTATC GTAGGGAGCC ACTTCTCCCC AGAGCAGACC CTTCTTGCCA GCCGGCCAGA 540
GTGGCTGGAG CCCCCTCCAT ACCTACCCAG GGAATATGGA AACACAGACA GTCATTTATG 600
GGGGGCTGAA AAGCTGATGT GGACCCCCAG CATGAAGATG ACCAGAAATG GGGTGAGGTG 660
TGGCCCCTCC CCTCCGAGGG CGGGGTTCTG GGTGGGTCCT GCTTCTCGGG GTGTGGGGCT 720
GCTTCCCTGG ATCAGGAAGG GCTGGAACTG GGCCCTGGGG TCAGGAGGAT GCGCAGAACA 780
GCTGCTGGGT CAGCAGTCTG GCGAAACGCC TTGTCCAGAC TTTATCAAGG CTGTGTGTGG 840
CCTTGGATAA TTCAGCACCT TCACCGAGCC TCAGTTGGCC CATCTGTAAA ATGAGATTCC 900
TGACCCCTGC TGTGTGGGCT GTTGTGAGGA GTAAAGGTGA AGACAGTAAG CCCTAACACA 960
CAGTAAGCCC TGACAGCAAA CAGGTGTTAG TGTTGAGAGA CAGCGTCCAC GGAGGTTGTG 1020
TGCTCTGACT CCAGTGTGGG GCTCTTAGGC TCTGAGCCTC AGTTTCCTCA TCTGTGAAGT 1080
GGGGTGATAG TGGCACTGTC CTCGGAAGAT GGTTGTGAGG ATTCAAAGGA TGCTGCATGA 1140
AAGACGCATG GCATGCAGTG GGAGGGTGAG AATGACACCG TGGCCTCCTC TGGCAGTGCC 1200
AGGAGCCCGT GGTGGGCACA GCTGGGCTGT CTGGCCTACC CATTGGGGCA TCTCCCACTG 1260
GGGTCTGGAG ACACCAGATC TGGGTCCTCA CAGGACTTGG GGCAAGTCCC TCGGCTGTCT 1320
GGTCCTCAGT TTTCCTCTCT GTGTGGTGGG GTAGGCAGCT CAGGTTCTCA GGCTCCCAAT 1380
GGCTCTGAGG AGGCAGCCAG CGTCACAGGG CTCAGGGCTG TGCAGGCGTC AGTGTGTGGA 1440
CAGACCTGCT GCTCCCGCCG CCCGCTCCTG CGCTCCCGCT TGCCTTCCTG AGCCACTTTC 1500
CGGCCTGTGG ATTCTGGGGC TGGAGGCCTG GATCCAGTTG GGGGCGCCTT TCCCTCACCC 1560
ACCGTGTGTT 1570
|
