Tag | Content |
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EnhancerAtlas ID | HS133-13695 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:79023250-79025120 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr17:79023912-79023923 | TGCCTGAGGCA | - | 6.02 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_25200 | chr17:79022511-79025155 | Colon_Crypt_3 | SE_26560 | chr17:79022179-79025369 | Esophagus | SE_31420 | chr17:79022257-79025350 | Gastric | SE_34261 | chr17:79015484-79025415 | HCT-116 | SE_36440 | chr17:79022176-79025537 | HMEC | SE_41709 | chr17:79023438-79025169 | LNCaP | SE_42160 | chr17:79015988-79025385 | Lung | SE_47416 | chr17:79021645-79027438 | Panc1 | SE_47964 | chr17:79023284-79024545 | Pancreas | SE_57453 | chr17:79022161-79025209 | VACO_503 | SE_65309 | chr17:79022165-79025391 | Pancreatic_islets | SE_69007 | chr17:79022537-79023808 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I081048 | chr17 | 79022188 | 79027464 |
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Enhancer Sequence | CTAGGTTTTT CTGGGTTTTT TGCACCTCTT GGTGTTGATA AGAAACAAGC TCCCTTCCCC 60 TTTTAAAGCC CACAGACTTT CCCGATCTCC TCCCCATCCC CTGCCCCAGC ACTGTCAGGG 120 CGTCTGGGCG TCTGAGCTCA GCTCCTTCCT GGTGGCATCC TGCAAAAAGA TACACTCGCT 180 CAGTGACTCG GAAAAGCCAC GTCGGTGTGG CTGAGAACAG AGTTCTTTCC ACCTGGGGCC 240 GCTGCTGTTG GTTTTCATTC CGGAAGAGCT GGAGCTGCCT GTCACTGGCT CCCCTGCCCC 300 CACCTGGGGA CCCCCAGGCA CTGCAAAGTG CCTGTTGGCT ATGGGCCCCC GGACCAGGAC 360 CTTGGCCTGA TTAGGGGAGC CGGAGGTGGA AGTGGAGGCG GGACTGGAGT GTATGCCCCA 420 CAGTGGGCTC TCCTCAGGCT GGGGACTTCC ACACGGGCCC ACTGGGTCAG GATGGCCCGT 480 GCCTGTGTTC TAGGATAATG GGATGGACTG GTTCGGAGGC TCAGAGAGAC GCCTGACCAG 540 ACGCCTGACT GGAGATGGTC TCCCAGCAGA GGGGCTGGGC TCTTCAGGGG CCACTGGGCT 600 CCTCCCGTGG TTCCTGGGAG AGGGAGGAAC CCGGAGGAGG GGTGGGTGGC ACCTACAGTG 660 CGTGCCTGAG GCAGGGCTCC ACAGAAGGCC TCTCTGCTGG CCCAGCGGCT GGATGCAGAT 720 GCAGAAGGAG GAACTGGCCC TTCCGCCCGC CCGGGAAGGG GAGTCCCCCC TTACAATGTT 780 GGCTCAGTGG GATCGATGCC TCTGCCATTG CCTTCGGGCC AGGACAGCAG CACTTGCGTG 840 TCCCGGCCGC CGCCCCTCTC TTGCAGATGG AGGCAGGGCC GTGCCCAGGT GTCCTGGTGG 900 CTGTTCCCTG CCCGCTGTCT CCTGCATTCC TTCCGTGTGA GCTCAGCTGC TGCACTAAGG 960 AAGCGAAACC TTGGTGCTGC CCCGTGCGTC ATGCGGTAGG CATGGCCGCC GTGCTGACCC 1020 GCCGTGGTTG GCCCTGGGTG GCTCCTGGCC TGTTTCTCCT GCTGCTCAGG ATGTTAGTGG 1080 AGCTCACAGG GCTCAGGTTG AGCCTCTTCC ACCCGGGGGC CTGTGGGGGT CATGGTCCTG 1140 GAGCCAAGCG CGTGGGGCTC TTGTGAGCAA GGGGTCTGCT CTGGCACGCC CACCTCCGTG 1200 GTAGTGTTTT CATACCTGTG TCACACAGGG TGAGAAACAT GCTTGATGCT GCAGCTCAGC 1260 ACACACACGC ACACAAATGT GCACATGCAC ACGTGGACAC ACATGCACAC ATGCATGTGT 1320 GTATGCACAC ATGGGCACAG ATGTGCATGC AGACATGAGC ACACGCACAC CAGAACACTA 1380 GAGTCGGCCG CATCCTCCTC ACTTGGCTGA TGCCCCCTTC TGCTTGATTT CATCACAAGA 1440 AACGCGCATC CGGCAGCATT TCCCGACCGC CTTCACCGCC AGTCCCGGTC TGCATGGTCA 1500 GTTTGAACCA GGCTGCCGAG AGCGCACCAG GTCCCAGCAT TCTCCTCTCT GCTGGTAACT 1560 CTTCAGGCAT TGTCTCTGGC TCACGTTCTC CTGGGCGCCA GACCTATCTC ACCCCACTCC 1620 CGGTGTGGCC TCCCTGCCCC GGCTCCCAGG CACTCCTGGG AGTTAAAGTG TCCAGGCTCC 1680 TGGTTCATTG CTGAGTGTTT AGCTCAGTGC TAACGCTGCT GTGCTCCAGC ATCCCCGTCC 1740 CTTTAGGACA GAGGCCTGCG TGGTACGTGC CTCTCTGCTC CAGCATCCCC GTCCCTTTAG 1800 ATCAGAGGCC TGCGTAGCAC ATGCCTCTCT TCCCCTCTGA CATCCCAGAG CCTCTGATGG 1860 GTCTCCCAGC 1870
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