Tag | Content |
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EnhancerAtlas ID | HS133-12236 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:8381950-8383420 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEOX2 | MA0706.1 | chr17:8382006-8382016 | GTTAATTACT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_01584 | chr17:8382501-8386445 | Aorta |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I008478 | chr17 | 8382301 | 8384830 |
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Enhancer Sequence | ATGTATTCCT CAATAGTGAC AGGTAGAATA AGTGCATTAT TCCTGCACGT GTAGGTGTTA 60 ATTACTGTAC ACAGGTATTC ATCATTGTAC TCAGTTATCT TACTTTGTTT GTTTTTGAGA 120 TGCAGTCTTG CTCTGTCGCC CAGGCTGGGG TGCAGTGGCG CCATCTCTGC TCGCTGCAAC 180 CTCCGCCTCC TGGGTTCAAG CAATTCTCCT GCCTCAGCCT CCTGAGTAGC TGGGATTACA 240 AGGCATGCAC CACCACGCTG GGCTAATTTG TGTATTTTTA GCAGAGACGG GGTTTTACTA 300 CGTTGGCCAG GCTGGTCTCG AACTCCTCAC CTCAGGTGAT CTGCCCGCCC TGGCCTCCCA 360 AAGTGCTGGG ATTACAGCCG TGAGCCAGCG CACCCGGCCT GTACACAGTG ATCTAAAGAG 420 CAAATGTTAC ATACAATCTA CCTGTCAGTT ATACTGAACA TAGACTTTTG AAGACACCAT 480 CCTTAGTTTA ATCACCTAAA CTTTTAGCCT GAGAAACAAC CCAATTTATT AAGTGATTGT 540 TTCACTTGAT AATTTACTAA TTACCTATTG TGATGTAGAG GGCTTTGGCA GCTCACATTG 600 AAAAAAAACC CAAAAACAAA CCCCCTACAC TCCCTCTTTG GTTAGAGGTG AAACAAATCC 660 ATGTTTCCAG ATGCATCTAC GTCGTCCCAT ATGAAGGAGA GGTAACTTAT TTGGAGGACT 720 CCATGGAAGA CAGAAAAAGT TATTTTGTTG CTTAACAAAT ATTATGCAAA AGTAGATAGA 780 GACAGTCAGC TGAAAGGGTG TTTATGTTAA TTCCAACTAG AAACAAACCC TTAATTGTTT 840 GCTTCAGCCC ACTGGAGTCC AAAGAATGGA GTGGGAAGTC CTGGCACGAG AGGCTGGGGA 900 GGATGCAGGG TTCTGGCCGC GAGCCCTGCA TTTCTGGGCT CCAAGCTCCC CAGCAAGAGG 960 GTGAATCTGA AGGTCTGCCC TGGCTCTGGG CGCTATGACC TAATAGCTTT GTAATATGCC 1020 TGCCAGCAGC TGTACTGTAC AATTTCTCAT CAATTTCAGA ATGCTTTAAT ACAACAATAT 1080 GAAAGCTGTT AAGCAATCCC TTCTATGGGG AGAAGAAAGG CTCTGATTTG TGTCATACTG 1140 CATTTGTTCT CTGGCAGCAA ATTAGCATTT CATGGGCTGC CACACGCTTG GGAAATCGAC 1200 TTTGGGTAGG AGATGCAAAC TCAGGGTGCC TAGGAAATCA CGGGGCGCCG TCCTAAAGCC 1260 CAGCCTTCCC TGACTGTTCA CGGATGCCGT CTGTCCTCCC AGGCTCTGAA TGCTCACAGC 1320 TCTTCTCTCA CAGCTCACAC CAACTTCTGT GTCCCACTCT GGTTATATGT GTTCTCTGCC 1380 CACGTGGTGG GGAGCCCCCC CGAAAGGGGC ATGCCTGTTT TGTCTCTGAC TGAGCCTAGT 1440 TGGTAAGTTT TGGTTTACGG TAGCAAAAAC 1470
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