Tag | Content |
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EnhancerAtlas ID | HS133-26267 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:10395370-10396840 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr6:10395395-10395406 | CATTGTTTATT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_47200 | chr6:10394387-10397986 | Panc1 |
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| Number: 2 | ID | Chromosome | Start | End |
GH06I010395 | chr6 | 10395581 | 10395817 | GH06I010397 | chr6 | 10396014 | 10396643 |
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Enhancer Sequence | TAACTAATTC TCTGCATTTG GAAACCATTG TTTATTATGA CCTTGTAATG TTCTAACCCA 60 CTATTTCCTT TCTGTCTTTC TCAGGATGCA AGGATTATAT TGGGTTCAGG TTTTCCAACA 120 TAACAAGCAT CTGTAAATCC AGATATGAAT GAATGGTATT TAATAAGATT GTTTTCGTTT 180 TAAAATGAGT ATTTATGTGT CATTGGAGGC AGAGCAGCAA TGTATGGCTG TTTATGAATG 240 CTATTGTGCC TGAGGTTAGG ATCCCCCACA CAATCTGAGA TGCAGCCAAG AAAAACAGCC 300 CTGATAGACA ATGCTTCACT TCACCTGCTA CAATGCTGTG TGCATTTCAT TTCTGTCAAG 360 AGTATGTACA GTTAGGGTTC ATTCGCCTCA TTATTTTGTT ACATCTACGT TACAGTTAAC 420 CAGTCTCTCT AGGAAATAAT AAATAACCGC TTTAAAAAAC AATTGCCGCG TTGCGTTCTG 480 AGAATACACT TTCCATTTGA ATTCTTTTTT AAACCCACCA TTGTTATGAA TTCTCTGGCT 540 TCGGAAAATA GAATTCAGAC TCCACCAACT CGCGTTCGTT TGTCGAGATT GATTTTACAC 600 TGCCTTCCAT AAGGAGATTA GAAAGCAAAA GGCTGCAAAA TGGACACTCT CTAATGCTTT 660 GCTTCCTTGG TCCTTCGGAA TGTCAGAGCG CAGGAACAAA TGTGAAATCC TACCAGTCTG 720 TCTACCTAGA CACTTGTTCT GTGGCCTTTC CTCTCAACCT TCCAGTTAAC CACCTCCTTT 780 TGCTTGTTAA AAATCCTCTT CACTTCCAAA GCAAAGAATT TCCAAATCAG TTTACAAAAG 840 CTCTGGATTC GCCATCTTTA TGCACAGGAA GTCCTTCCTT CTCTCAGAGC TCAGCACACA 900 GTCCTCTTAT TGTAGAAGAC AGATAGGAGA GGTCTGGAGA GGCAGGCTTC ACAGCCCTCC 960 CCCATCCTCC CCACCCCACC TCAGAGAACG TTTTGTATTT CTAAAAGGTT CTAAGAGGAG 1020 CCCTGTGGTG ATAGGAAGGG GTGGGCTGGC ATTTAGGGGC AAGCAGGAAA GATTCCAGGG 1080 ATCAACATCA TTTCCCACTC CCCTCTCTAC CTCGAGAGCT ACTGAAGAAC AGCACAGTAG 1140 TAAATTCATC TCTAAATAAA ATATGAAAAT AAATGGGAGA CAATTTGCCC TCTCTTTCCC 1200 TGCTACATGT ATATTTCTGC CACTATTCCT TTTCTCCCGC CAGAAATCTA GAGCTGGTCT 1260 GAGCTCATTT GCCCGTCTTA GCCGCTGACT ACCCTGAGCA AGCAAGTGAA GGTTGAAGTC 1320 GGTATTTCCT TTGTGCTAAT GAACTAACAA TTTAAATCTC AGTTATCCTC TGAGACAAAT 1380 TCCAAAGCAG TTATGGGGGG CGGGGGGGGG GGCTGTTAGG CGGGGGGCCT GCTGGTGGGA 1440 AGTTTCTTCT GTTCTTCTCC ATCTTCCTTG 1470
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