| Tag | Content |
|---|
EnhancerAtlas ID | HS133-19811 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:60771010-60772900 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr20:60771206-60771218 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr20:60771739-60771751 | AAACAAACAAAC | - | 6.32 | | MEF2A | MA0052.3 | chr20:60772287-60772299 | ACTAAAAATAGA | + | 6.27 | | MEF2B | MA0660.1 | chr20:60772287-60772299 | ACTAAAAATAGA | + | 6.32 | | MEF2C | MA0497.1 | chr20:60772285-60772300 | CTACTAAAAATAGAA | + | 6.57 | | Nr2f6(var.2) | MA0728.1 | chr20:60772236-60772251 | GAGGTCAGGAGTTCA | + | 6.22 | | TFAP2C | MA0524.2 | chr20:60771010-60771022 | TGCCCTGGGGCA | + | 6.44 | | TFAP2C | MA0524.2 | chr20:60771010-60771022 | TGCCCTGGGGCA | - | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGCCCTGGGG CAGTGCAGCG GGGTTGAGGA GGGGCCCCGA GACTGCATGT GCATTTGAAC 60
TAAAAACCTG ATGTATGGGC AGGCACAGTG GCTTATGCCT GTGATCCCAG CACTTGGAGA 120
GGCTGAGGCA GGAGGATCAC TTGAGCCCAT AAGTTCAAGA CCAGCCTGGA CAATATAGCA 180
AGACCATGTC TTTTTTGTTT GTTTGTTTTT TTGTTTTTTT TTTTTTGCCT CAAGGTTTGT 240
GGATCTACAA AAAATTTTTG AAAAAATTAG CCAGACATGG TAGCGTGCAC CTGTGGTCCC 300
AGCTACTCAG GAGGATTGCT GGATCCCAGA AGTTCAAGGC TGCAGTGAAT CGTGATCACA 360
CCACTGCATA TTCCAGCATG GGTGACAGAG CAATACCCTA TCTCTAAAAA AAAAAAAAGT 420
AAAATTTTTA AAACCCAGCT AGGCGCAGTG GCTCATGCCT GTAATCCCAG AACTTTGGGA 480
GACCGAGGCG GGTGGATCGC TTGAGGTCCG GAGTTCGAGA CCAGCCTGGC CAACGTGGTG 540
AAATCCTGTC TCTTAAAAAA TAATAATAAT AACCAGATGT GGTGGCACAC ACTGATAGTC 600
CCAGCTACTT GGGGCTGAAG CAGGAGGATG GCTTGAGCCC AGGAGGTCGA GGTTGCAGTG 660
AGCTCCGATT GTGCTGCTGC ACTCCAGCCT GGCCAACAGA GGAAGACCCT ATCTCAAAAA 720
AACAAAACAA AACAAACAAA CAAAAAAAAC CCTGATGTAT GGATATCATT TTTATAAATT 780
ATATGGATAT TCAGCCGGGC GTGGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGACC 840
GAGGCGGGTG GATCGCTTAA GGTCAGGAGT TCGAGACCAG CCTGGCCAAC ATGGTGAAAC 900
CCCGTCTCTA CAAAAAATAC AAAAAAAATT AGCTGGGCGT GGTGGTGGGC ACTTGTAATC 960
CCAGCTACTA GGGAGGCTGA GGCAGGAGAA TTGCTTGAAT CCAGGAGGCA GAGGTTGCGG 1020
TGAGCTGAGA TCGTGCCATT GCACTCTAGC CTCGGCAACA AGAGTGAAAC TCCGTCTCAA 1080
AAAAATAAAA ACATAAAACA TAAAAAAAAA ATTATATGGA TATTCATAGT TAAGTAGCAC 1140
ACCCAAAAAA GCAACTTTGA GGCCAGGCGC AGTGGCTCAT GCCTATAATT CCAGCACTTT 1200
GGGAGGCCAA GGCGAGTGGA TCACCTGAGG TCAGGAGTTC AAGACCAGCC TGGCCAATAT 1260
GGAGAAACCC CATCTCTACT AAAAATAGAA AAATTAGCCA GGCGTGGTGG CAGATGCCTG 1320
TAATCCCAGC TATTTGGGAG GCTGAGGCAC GAGAATTGCT TGAGCCCAGG ACACAGATGT 1380
TGCAGTGAGC CAAGATCATG CCACTGCACT CCTGCCTGGC TGACAGAGCG AGACTCTGTC 1440
TAAAAAAAAA AAGAAAAAGC AACTTTGAAC ATGTTTTGTT TTGTTTGTTT AATTTCAGGA 1500
GCACAGAGAG TTTCCTGTCA GGGAAGCTGA CATGTCGGTC GCGTGAAAGC ACGAGGCCTG 1560
TGTGGTGGGT TCGGTGGGTG CCGCTGGCTG CTGGTTATAT TCACACTCAG CATAGACGCA 1620
TAGCGAGCTG GGAGTGAAGC CTTCACAACA AAAGCATAGA ATACAGCTAC TGTAAAAAAT 1680
AAGAAATTTA AAAATTTTCA GAAATGATAG CACTTTTTGA AGGAAAATAA GGATTTCATT 1740
TTTAAAAAAT CACTTTGCTG GTTTTGTAAC TTCTGCTGCA CCCTCACTCC ATGCTTCCAT 1800
ACCTATTTTT AAGGTTCTTA AACTGGACCC AGACACATCA GCAATAGGCC ATGGTTGTCG 1860
TAACACAAAG GGACTGAGAT TCTTGTTCTT 1890
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