Tag | Content |
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EnhancerAtlas ID | HS190-05688 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr17:73119970-73121280 |
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 | ACTCCAGCGT GGGCGACAAG AGCGAGGCTC ATACTCAAAA AAAAAAGTAC TGTATACTGT 60 TTCATCATAT GCATGTACCA TAATTTAGCC ATCTGGCTAT TACCAAGCAT TCTAGGAAGC 120 TCCCAGTTTC CACGTTGCTC TTTTTCCATG GCCCTTCTCA GTTCTTCAGG GCAGGTTCAC 180 ACAGGTAGAC CCAGGGAGAA GCTCAAAGCA GCTGTTGCTG TGGCCTCTTG TGGGTCCTCT 240 GGCGCCATCT TGGCTCATCT TTCTGCTCCA GCTCAGACTT CCTGCCCTGA AACTCTGTGC 300 CCTTTTCTTT TCTGGCCCTC ACCGCCTTCT TCATCTCTAA GGGACACTAC CCGCTAGGCA 360 GAGGAGCTTC AGGAGTTCCC TGCCACTGCG GAGAGGGTCC AAGCAGCTGG TGAGCTCTGG 420 CAGGCACCCG GTCCATCCTT GGAGACTCCT AGGCCTCTGT GTGGGGAGGG AGGGAGAGGG 480 TGGCTCTCCT GAGGCCTCCT CCTGCCCCCA CCCTCTGGTT TTCCGCAGTC TGGGTGGCAG 540 TGCCCTGCCC AGGCGCACCT GGGTGTGGTG ATGACTCAGC TGCCAGGCAG TGACTCAGGC 600 TTCATCTTAT CACACTTTAC ACAGAGAGAA ATCCCATCAC CCCACCCGCA GTCCAGTGTG 660 CACAGGAAGG CCGCTCCCGT CAGCTCGGGA GACATGCCGC GGGTGTGTCT GAGCAGAAGA 720 GTCCGACCAC AGCACTTCCA CTGCCCCTGC TCCAGACTGA GCCTGGCATC TGCCCAAGGC 780 TGGATTCGTT GTCCTTACTG CTTCCAGAGG GCCCCGCCAT TTCCCATGGG AGGGCCGCCA 840 TTTCCCATGG GAGGGCCGAG GGGCAGAAGG CTCCCATCTC TTTAGCGTTT TGGGCAGCTC 900 ACTCAGTCTC TCATAGCCTT GACTTCTCCC ATGGAAATGG GGGTGATGTT AGCACTTGTT 960 TCTAGGGTTC AGTCATGTGT CCAGTGCGTG CTCAGTGAAG TGTCCACGGT TCTAGGAACT 1020 TGAGCCCTGC CTTATAGCTC CTGGTGGAAG GGACAGAGCA AGGACAAAAG GCAGCCTACA 1080 GAATGCCACA GCCACGCTAG GGGCCACCCT GTGCTTTAGC AAGTGCTGAA GTGGGACTGG 1140 CAAGGGAGGC TCCAAGGGCC CCATGGGGAG AGGCGCTCAG TCAGGGCCTG CTTGCCCTCT 1200 GCTGCTGCTA CTCTTTCTCA GGACTCCAGA GAGGCCAAAG AGCTCCTTCC CTCCCTCAGA 1260 TGTGTCCTGC CTGTGAGCTG CAGCCCAGAT CTAAGAACTA CAGAAGTCCA 1310
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