Tag | Content |
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EnhancerAtlas ID | HS083-01117 |
Organism | Homo sapiens |
Tissue/cell | HCC1954 |
Coordinate | chr17:73119960-73121240 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr17:73120176-73120189 | AGCAGCTGTTGCT | + | 6.59 | SREBF1 | MA0595.1 | chr17:73120605-73120615 | ATCACCCCAC | + | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_24792 | chr17:73119901-73121732 | Colon_Crypt_3 | SE_31669 | chr17:73119896-73121748 | Gastric | SE_49028 | chr17:73119945-73121764 | Right_Atrium | SE_50894 | chr17:73119726-73121747 | Sigmoid_Colon |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 73120387 | 73120767 | chr17 | 73120050 | 73121043 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I075123 | chr17 | 73119574 | 73122496 |
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Enhancer Sequence | GTGCTACTGC ACTCCAGCGT GGGCGACAAG AGCGAGGCTC ATACTCAAAA AAAAAAGTAC 60 TGTATACTGT TTCATCATAT GCATGTACCA TAATTTAGCC ATCTGGCTAT TACCAAGCAT 120 TCTAGGAAGC TCCCAGTTTC CACGTTGCTC TTTTTCCATG GCCCTTCTCA GTTCTTCAGG 180 GCAGGTTCAC ACAGGTAGAC CCAGGGAGAA GCTCAAAGCA GCTGTTGCTG TGGCCTCTTG 240 TGGGTCCTCT GGCGCCATCT TGGCTCATCT TTCTGCTCCA GCTCAGACTT CCTGCCCTGA 300 AACTCTGTGC CCTTTTCTTT TCTGGCCCTC ACCGCCTTCT TCATCTCTAA GGGACACTAC 360 CCGCTAGGCA GAGGAGCTTC AGGAGTTCCC TGCCACTGCG GAGAGGGTCC AAGCAGCTGG 420 TGAGCTCTGG CAGGCACCCG GTCCATCCTT GGAGACTCCT AGGCCTCTGT GTGGGGAGGG 480 AGGGAGAGGG TGGCTCTCCT GAGGCCTCCT CCTGCCCCCA CCCTCTGGTT TTCCGCAGTC 540 TGGGTGGCAG TGCCCTGCCC AGGCGCACCT GGGTGTGGTG ATGACTCAGC TGCCAGGCAG 600 TGACTCAGGC TTCATCTTAT CACACTTTAC ACAGAGAGAA ATCCCATCAC CCCACCCGCA 660 GTCCAGTGTG CACAGGAAGG CCGCTCCCGT CAGCTCGGGA GACATGCCGC GGGTGTGTCT 720 GAGCAGAAGA GTCCGACCAC AGCACTTCCA CTGCCCCTGC TCCAGACTGA GCCTGGCATC 780 TGCCCAAGGC TGGATTCGTT GTCCTTACTG CTTCCAGAGG GCCCCGCCAT TTCCCATGGG 840 AGGGCCGCCA TTTCCCATGG GAGGGCCGAG GGGCAGAAGG CTCCCATCTC TTTAGCGTTT 900 TGGGCAGCTC ACTCAGTCTC TCATAGCCTT GACTTCTCCC ATGGAAATGG GGGTGATGTT 960 AGCACTTGTT TCTAGGGTTC AGTCATGTGT CCAGTGCGTG CTCAGTGAAG TGTCCACGGT 1020 TCTAGGAACT TGAGCCCTGC CTTATAGCTC CTGGTGGAAG GGACAGAGCA AGGACAAAAG 1080 GCAGCCTACA GAATGCCACA GCCACGCTAG GGGCCACCCT GTGCTTTAGC AAGTGCTGAA 1140 GTGGGACTGG CAAGGGAGGC TCCAAGGGCC CCATGGGGAG AGGCGCTCAG TCAGGGCCTG 1200 CTTGCCCTCT GCTGCTGCTA CTCTTTCTCA GGACTCCAGA GAGGCCAAAG AGCTCCTTCC 1260 CTCCCTCAGA TGTGTCCTGC 1280
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