| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00549 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:20436520-20437840 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr1:20437456-20437467 | AATGAGTCACA | - | 6.62 | | Foxd3 | MA0041.1 | chr1:20437173-20437185 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:20437177-20437189 | AAACAAACAAAC | - | 6.32 | | POU4F2 | MA0683.1 | chr1:20436522-20436538 | TTCATTCATTATTCAT | - | 6.17 | | RREB1 | MA0073.1 | chr1:20436841-20436861 | CGGTGGGTGGTGCTGGGGGG | - | 6.28 |
|
| | 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 |
| GH01I020109 | chr1 | 20436265 | 20438010 |
|
Enhancer Sequence | GATTCATTCA TTATTCATTT ATTTGTTCAA CAAATCCCTA TTGATCACCT ACTACATATC 60
AAGCCTGCCC TGGTGATAAG GTGGTCACAG ATGGGAGCAC CCCAGGCACA GCTCTGCTCC 120
CAGCCAAAGT GAGAGCGGGT TGCAGTCCCT GGCTCTGGGC TTGCTCGCCC AACACAAATT 180
CCATCAGCTA CCCAACCCCT CAGGGACATT GATCCTGTTC CGTCTTGGGG GTAAATAAAT 240
CCTAATGAAT CTAAACCAAC CAGGCTCATC CCATTGTCTT GGGTAACCTC TGGGTTAGGG 300
CGGCCTGTCC TGAAGAGAAG TCGGTGGGTG GTGCTGGGGG GCTTATTAAA AAGACAGAGG 360
AGGCCGGGTG GGGTGGCTCA CACCTGTAAT CCCAGCACTT TGGGAGGCCC AGGCAGGCGG 420
ATCATGAGGT CAGGAGATCG AGACCATCCT GGCTAACATG GTGAAACCCT GTCTCTACTA 480
AAAATACAAA AAATTAGCCG GGCATGGTGG CGGGCGCCTG TAGTCCCAGC TACTCGGGAG 540
GCTGAGGCAG AAGAATGGCT GGGAGGCAGA GCTTGCAGTG AGCTGAGATT GCGCCACTGC 600
ACTCCAGCCT GGGCAACAGA ACGAGACTCC GTCTCAAAAA CAAACAAAAA AGCAAACAAA 660
CAAACAAACA AAAAGACACA GGAAGAGAGG AAGACACAGC GTCTCCTTGG CTGGATGCTG 720
TCACGTCCTG GCCTGCGGGC TGGCATCATG GTTGCCAGCT TGGAGCTGTG AGGGGAGTCA 780
CCTAGAGGGC AAAGCCAACA CACAGAGGTG GCTTGCCAGG AGCAGGAAGG AAACCAGGCC 840
CTGATGATAT CAAGCTCCGA AGAGCCAGAC TTGGAACCAC CTCCTCTCCG AACGTCTCAT 900
CATGTGAGAT CATAAACGCC TGCATTGTTT CAGCCCAATG AGTCACAGTT TTTAGCTGGA 960
AGCTTCTTAA CCAATACAAA CGTGATGCGG CGAGGGAGCG GAGCAAGAAG AGGCTGGGGC 1020
GAAGCTGTGG CTCTGCCTTT CTTGGGTTGT GGGACCTCAG GAGGGTCCTC AATTATAAAA 1080
TGGGGATCGT AATGGCTAAG TCAGCCAACA TGAATATTAA GAGAGATGTT GCTGCAAAGC 1140
CATAGGGAGC TATTGGGCCA AATTTGGTAG ACAAATAAGA GTCATCAGCT CCCGATGGTG 1200
TCTCTTGAGT AAATGCATCC AGTGTCACTG AGAGAAGACT TGGCGGGAAA GGAGGAGGAC 1260
ACTTTCTCCT CCTGATTTCT CTTGGGGGTG ACTTTAGATC TGGTCACTAC GAAACAACAA 1320
|
