| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21969 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:12771530-12772700 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr3:12771839-12771850 | TGTTGTGCAAT | - | 6.14 | | HES2 | MA0616.2 | chr3:12771614-12771624 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr3:12771614-12771624 | GGCACGTGCC | - | 6.02 | | MEF2A | MA0052.3 | chr3:12772633-12772645 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr3:12772633-12772645 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr3:12772632-12772647 | TTCTATTTTTAGTTC | - | 7.13 |
|
| | 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 |
| GH03I012727 | chr3 | 12769309 | 12772299 | | GH03I012730 | chr3 | 12772461 | 12772602 |
|
Enhancer Sequence | CGAGGTCAGG AGATCGAGAC CATCCTGGCT AACAGGGTGA AACCCCATCT CTACTAAAAC 60
TGCAAAAAAT TAGCCAGGCA TGGTGGCACG TGCCTGTAGT CCCAGCTACC CAGGAAGCTG 120
AGGCAGGAGA ATCGCTTGAA CCTGCGAGGC GGAGGTTGCA GTGAGCCGAG ATGGGGCCAT 180
TGCACTACAG CCTGGGCGAC AGAGCAAAAC TCTGTCTCAA AAAAAAAAAA AAGTGGTAAA 240
ATAGACATAA AATTAACCAC CATAACCATT TTTAAGTGTA CAGTTCAGTG GCGTTAAATA 300
CTTTCACAGT GTTGTGCAAT TATCACAACC ATCCATATCT AGGGCTGTTT TCATCTTCCC 360
AAACTGACAC TCTGTCCCCA TTAAACACTA ACTCTCATTC CCCGTCCCGC AGCCTCTGGC 420
ACCCACCATT CCACTTTCTG TCTCTATGAA TCTGATTACT CTAGGTACCT CATATATATG 480
GAATCATAAC TGTATTTGTC CTTTTAACAT AATGTTCTCA AGGTTTATCT GTGTGGTAGC 540
ATGTGTCACA ATTTCTTTTT TTTTATTTTT ATTTTTTTCT TAGAGACAGA GTCTTACTCA 600
GCCACCCAGG CTGGAGTGCA GTGGCATGAT CATGGTTCAC TGCAGCCTCC ACTTCCTGGG 660
CTCAAGTGAT CCTCCCACCT TAGTCACCTA AGTAGCTGGG ACCACAGGCA TGTGCCACCA 720
CGCTTGGCTA ATGTTTTTAT GTTTTGCAGA GATGGGGTTT TGCCGTGTTG CCCAGCCTGG 780
TCTTGAACTC CTGGGGTCAA GTGATCCTCC TACCTCAGCC TCCCAAAGTG CTGACATTAC 840
TGGCATGAGC CAGTATGCCT GGCTAGAATT TCCATATTTT CCCCCTTTGG TTTTTATTTT 900
TTTGTGAAGT CTCAAATAAT TTCCTTTTTT AAAAACTGAT AATATACCAT GCTTTGTTTA 960
TTCATTCGCC CATTGATGGA CGCTTGTGCT TCCCCTTTCT GGCTACTGGA AATAATGCTG 1020
CTTTGAAAAT GTGTGTACAG AGATCCCTTC AAGTCCCCTT TGGGCATATG TGCAGAAGTA 1080
GAACTGCTGG ATCATATGGT AATTCTATTT TTAGTTCTTT GAGGAATCAC TATACTCTTT 1140
TCCATAGCAG AAGTGGAAAT TTAAAAAAAA 1170
|
