| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26112 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:2658080-2660600 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr6:2660326-2660337 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr6:2660326-2660337 | GGTGACTCATG | + | 6.02 | | SPI1 | MA0080.4 | chr6:2659300-2659314 | CACTTCCTGTTTTT | - | 6.36 | | mix-a | MA0621.1 | chr6:2658526-2658537 | CCTAATTAATT | - | 6.32 |
|
| | 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 |
| GH06I002658 | chr6 | 2658757 | 2660635 |
|
Enhancer Sequence | GGACATCAGG ACTTTACCCC GGGTTGGGAA GGATGGTGCG ATTTTGGTGT TTGTCAGGTA 60
AGATTAGTGG AAAATATTTT AGACAAAGAG AAGAGGATGT ATAAAGCTTG AGAATTATAA 120
ACAAGACTAT TGTACTGATG TTGTCAGGAT TTGACAATAC TCAGAAGAGT ACCACCATAA 180
CAAAAACCTA AAAGGTGGGA GAGACATTGG AACTAGGCTG TGGAAATAAG CTGGAAAGAC 240
TTTGAGAAAA GTATTAGTGA AAGCTTGAAG AGGCTTGAAG AGTGTTTCAT GACATCTTAA 300
TGATCTTTGA GGAGGTTGTG AGTGAGAGTT TGAAGAAAAG TAAAGAAAAT TTTATTTGAA 360
ACTGCAGAAA AAAGATTTTT GTTATATTGG TGGTAGAAAG TTTAGCAACA CTGTCATCTG 420
CAATAATAGA GAAAGTAGAA AATTTACCTA ATTAATTGTG TGATCTAACT AAGGATGTTT 480
CCAGAGAGTG CTGAAACTCT TCCAGGTTTC TTTTTGCTGC TTATAATAAA ATGTGAGAAG 540
AAAGAGATAA ACTAAAGGAA GGACTTTTAA AGAAAAAATA TATTTAAAAA AAATTCCAAC 600
CTCTAGGGAC AACAAATGAT GGTACAATTA AGAAATGACT TCCAGGTAAA GATCAAATCC 660
AGGACACGCT AAAGAAAACA TGGTCTAAAC ATGAAGCCAA GAATTTAAAA TTATTTGTTA 720
AGACTTCAGA AATATTCAAG ACAGTGCATT AGAGAATTAT TCAGTCAAAC AATAGGGCTT 780
CCAAGGTGTT TAAGGGTGTT GGCCCTCAAC AGGCCCAGCA GAAGTCCAAG GTAAAGAAGA 840
GCTTATCTTG AATGGTGAGT GCAGTCCTTC TCTAATGAAG TGAACCTCAG TAAAATTCGC 900
AGGAGGTCTA GAAAGTTTTG ATTTACATTG CTTGAAGCAC CACCAGTTTG GACTGACACA 960
GGCAACAACC ACAAAGAGAA AAGAGGCCTT TGTCCTCCCA AACTATTCCA CCAGCAGGAA 1020
GTAAGTTGAG AAACCTACAC TGCCACATGC AGAGACTAGC CTTCATGGAA AAGGGAGAAT 1080
GACTCAGAAG GTGAAAGCGA GAGTCCAGAG GGTGGATCCA GGAGTGGGTG ACCGTGCCTT 1140
GCATGGAGAA GGACATGTGT CATTGGGGAG CTGGGGATAG ACAATGATCA CTGACCTACA 1200
AAGTAGTCCC CAGTGATTCT CACTTCCTGT TTTTCGTACC TTGTATAGTC CCCTCCCACA 1260
CTGAATAGGG CATCATGGAA ATCAGAGAGT GTGACGGCTG CTTGGGGTTA GGACATAAAA 1320
ACGTGGAGAT TCCTGTCTTA CTCTCTCCTC GATCACTCAT TCTGAGAAGC CAGCTGTCAC 1380
ACGATCAGCC CTATGGAGAG GTCCACCTGG TGAGGAAGGG AGGCCTCCTG CCAACCACCT 1440
CAGCATCAAT TTGCCAGCTA TGCAAGCGAG CCATCTGGGA AATGGATCCT CCTGTCTCAG 1500
TCACGGTCTT TGTTGGCACT AGTTGTGATA AAGAGAAATA ACACTACAAA TTGTTCCGAA 1560
GCCTTTGTTA GTGCCTGAAT ATTCTAAAGG CATTCAAATC CGAAATTTCA GCAGTCATGG 1620
TGTCCGAAAA GATCCACATC TGTAGGCCAA CTTGGGCTAG GGATGCCGTA TTAGGACCCT 1680
GCTGGAGGCC TAGGACATCA TTCCTGTGTC TTTAGTGTGG AGCAGGATGG GAAACATCTG 1740
GCAAATGACA TTGAAAAGTA AGGCCAGCTG CATGAACAGG CATCTTAAAC ATGACGCTAA 1800
GAAATTCAAC ATTTTTTGAG CCTAAGTTTC TGACCTTTAA AGTTATCTGA TTAGATTTGT 1860
CTTTTAAAAA TAAAAAGATC ATCAGTGTGG AGGAGACTGG AGAAGAAAAA CACAGCAGTC 1920
CAGTACACCA ATGATGAAGT CCAGTGAGAT CTATGAAGTA TGAGTGTATC CCAGCCAGGG 1980
CCCCCAACAA CGAAATGGGG GATGAGGGAT GGAGAAGAAG GAGCCAGACG GTTACTTGAG 2040
GAGGGTATTT GCTCATCACT AGTTCAGCTC TCCACAGAAA ATCGTGAGAT CTTAGTTTTA 2100
AGAGAAATGG GAACTCAGAA GGGCCAGTCC TCTGGAAGGG ATGGGCATGG CCCTAGATCC 2160
TTCCTTGCTG CTTCATAGCT GCTTGAGGGG CCTGCATCAT CAGACTGTTA AGAATGACAG 2220
CAAGTGCTCG TATGGAATGG TTCTGTGGTG ACTCATGGGT GCCAGCTGAC TCTAGAAAGC 2280
AGACAGGCAC TATAGGTAAA GGGCAGGGAT TCAGACAGGC CTGATGGGCT TTCTGAGATG 2340
TGTATTTTGG GGGAACAAGC CTTCACGGGA GTGAAAGAAG AGCAAAGAGA TGTGTGGCCC 2400
ATTCTCAGGG ACTTGTGTGT TCCTCAACCC GCTACCTGAG GGGCCAAAGG CAGAGCTGAA 2460
GAGCTTTTTT CAGGAAGGAT TGTGCGAGGT GCTGTGGCAA ACAGGATGAG TTTGTCCATG 2520
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