Tag | Content |
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EnhancerAtlas ID | HS139-23017 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr17:39803620-39805790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:39804312-39804331 | GAGCGCCCTCTGCTGGCCA | - | 8.64 | HEY2 | MA0649.1 | chr17:39804652-39804662 | GGCACGTGTC | - | 6.02 | HSF1 | MA0486.2 | chr17:39803951-39803964 | GAACTTTCTAGAA | - | 6.41 | Npas2 | MA0626.1 | chr17:39804652-39804662 | GGCACGTGTC | + | 6.02 | SREBF2 | MA0596.1 | chr17:39805381-39805391 | ATGGGGTGAT | + | 6.02 | ZNF263 | MA0528.1 | chr17:39803843-39803864 | GAGGCAGGGTGAGGAAGGAGA | + | 6.04 | Zfx | MA0146.2 | chr17:39804514-39804528 | CAGGCCCCGGCTGG | - | 6.11 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_03031 | chr17:39804348-39804984 | Bladder | SE_23072 | chr17:39804178-39805461 | Colon_Crypt_1 | SE_23072 | chr17:39805543-39816268 | Colon_Crypt_1 | SE_23729 | chr17:39804285-39805404 | Colon_Crypt_2 | SE_24709 | chr17:39804129-39805405 | Colon_Crypt_3 | SE_24709 | chr17:39805528-39806106 | Colon_Crypt_3 | SE_26572 | chr17:39804188-39805339 | Esophagus | SE_26572 | chr17:39805512-39817935 | Esophagus | SE_28152 | chr17:39804166-39805384 | Fetal_Intestine | SE_31558 | chr17:39804294-39805454 | Gastric | SE_33881 | chr17:39804203-39805423 | HCC1954 | SE_35148 | chr17:39803583-39814501 | HeLa | SE_35867 | chr17:39803719-39814849 | HMEC | SE_50351 | chr17:39803561-39805415 | Sigmoid_Colon | SE_50351 | chr17:39805502-39813786 | Sigmoid_Colon | SE_52437 | chr17:39804214-39805417 | Small_Intestine | SE_55466 | chr17:39804556-39804992 | Thymus | SE_57399 | chr17:39804201-39805123 | VACO_503 | SE_57969 | chr17:39804383-39805089 | VACO_9m | SE_64297 | chr17:39803480-39816383 | NHEK | SE_65870 | chr17:39803512-39806328 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 39803709 | 39803800 | chr17 | 39804380 | 39805400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I041647 | chr17 | 39803658 | 39805837 |
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Enhancer Sequence | GAGGTGGAAG GCAGAATTCA CAACCGAAGG GATTTTCTCC TCCCTAGTCG CCTCCCCCAG 60 TAGTTGATGG CGGCTGCCAC ACCTCAAGCC AAGCAGGGGA CCTGGCAGTG TTCACCCGCC 120 AGCTGCGTGA ACGCCCGTAA CTCTTTACGG CAGAAGACCA AGGGTGCGTC TGGTCCTCAG 180 AACTGCAGGA TGCACCGGCA GCGATGGAGA AGCCTCCTTG GATGAGGCAG GGTGAGGAAG 240 GAGACCAGAC AAGCAAGTCC TCCTCCCAGA GGCAGGGACA GGAAGCAGGA GCAAGGGGCC 300 ACCAGGGAAG CTGCAGGGGC TAGAACCCAG GGAACTTTCT AGAAAGGCTA GCTGGCCCTA 360 ACAGACCCCT GGCCTGGAGG AAGACCTCCA GGGCAGGTTA GGCGGGCCAG TCACATCTCC 420 GGGGGTGATT TAAAAGGCAC CACCTTGGGA CAAAAGGATG GAAGCATTGA CCAGACAAAT 480 GCCTGACCCG GCAGCAGCAG AAAAGGATGC ATGGAACCCT GTGGGGTTCC CACCTCATGA 540 GGTCGTCTCT CCTCATTCTT GTGCTCGGTG GCTCCCAAGG GGCAGGCTCT AGTGCTCCCC 600 ATGGAGACCC CAGGCCCAGC CGCCTTCCAA GGCTCATGCC CTGTTAAACG GGGACACGCT 660 CCGGCCGCCC GGGATCCCCA AATCTGTAGC AGGAGCGCCC TCTGCTGGCC ATCTTGGGTG 720 GCGCCTCTGC GCTGCAGTCC CGAGAGGAGC CCGCGAGGCC GCGGGAGGAA TGCAGGGACC 780 CTGGAGACCC ATCCTCCACC TGCGCTCTGC AAACTACTCC TTCTCCCCCA GGGTCCTGGC 840 TCCTCCTCGC CATCTTCAGC TTCACCGTCT CTAGTCCCTT AACAGCCAGA GCACCAGGCC 900 CCGGCTGGGC CGTGTGTCCA TGCCTCTGCC TCCAGGCGCA TGGACACAAC ATTCCCTTCT 960 GAAGCTGGCC TGCGCTGTGT ATCACCCCCT ATCCCCCATC CCTCCATCTC AAAAAAGCCC 1020 TTCCCTGCCT TTGGCACGTG TCCCTCCCCC ACGCCCACCC GCTCAAGTCC CTCTGTTAAT 1080 AAACTGCTAA CCCCAAAACC AGCCTTCCCT CCAGCTTGCC CGGCCCCGAG TCTGAGGGTC 1140 CCTGGAGCAG ACACGCTCCA CCCGCGGGGA CCTCTCCCTC CTGTCAACTC CTGAGGAGCG 1200 GCAGCGGCTT CTGGGCTTCC CACGCGGGGT GTGACACCAA CGGGGGACAT AATACAAACG 1260 AACGAGGGTA AAGTCCGTGT GCACACCTGT GCATGGCCAC ATGCGGATGT GCGTCCAGGC 1320 GTGCCTTGCA GGTGTGTGGG CAGTGACTGC GCCCACCCCT CTGTCGGGTC TCGCCACGCT 1380 TAGCTGGGTG GGCTCCTTCC AACCCAGGCT GGGGCTGAGC AGGAGGAAGC CGCGGCCTCG 1440 CCCCCAGAGG GCAGCACTGA GCTGTTCTGG CCCGACTGCT GCCAGACTCT ACCCGGAGAG 1500 GAGTCCTGAG TTTCCCCGTC CAGGGCCTGG GGGAAGGACT TCAAATCTGT AAAGGAAAGC 1560 AAGGAATCAA ATCCCAAATC CAGGCTAGCG GTTACACTGC GGGCAGAGCG CGAGGCGCAC 1620 ATCGAAGCTA AAATGTCCAA AATTGGGCAG TGGATTCACG GATGTTTGTT GTGCTTTTAT 1680 TCTTTTTTTG TTTTTTTCTT TTTTTTTTTT TTTTTTTTTT TTGAGGTCGA GTTTCACTCT 1740 TGTCGCCCAG GCTGGAGTGA AATGGGGTGA TCTCGGCTCA CTGCAACCTC CACCTCCTGG 1800 GTTCAAGCGA TTCTCCTGCC TCAGCCTCCC AAGTAGCTGG GATTACAGGC GCCTGCCACC 1860 ACGCCCGGCT AATTTTTGTA TTTTTAGTAG AGACAGGGTT TCACCATGTT GGCCAGGCTG 1920 GTCTCGAACT CCTGACCTCA GGTGATCCGC CCACCTCGGC CTCCCAAAGT GCTGGGATTA 1980 CTGGCGTGAG CCACAGCGCC CGGCAGTGCC TTCATTCTTA AATCCTACAC ATATTTTGTA 2040 AATATTATTT TGAATCTATT CAGTATTACT CTTTTCAAAA TAAAGGCCTC CGAGCCCTCT 2100 CTAGAATGTG GAAAGACCAC TCATCGCTCA GTGGAGCAAA GTGAGCCTAC AAGCTCCCCA 2160 GATCGCCCCC 2170
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