Tag | Content |
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EnhancerAtlas ID | HS108-17765 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:73548760-73550040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr17:73549938-73549948 | CTCAAGTGGT | - | 6.02 | Stat6 | MA0520.1 | chr17:73549193-73549208 | CTTTTCCTGGGAAAT | + | 6.57 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_23798 | chr17:73548877-73549188 | Colon_Crypt_2 | SE_28701 | chr17:73548364-73550101 | Fetal_Intestine_Large |
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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 |
GH17I075552 | chr17 | 73548227 | 73550051 |
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Enhancer Sequence | GGATGATTTA CAGTGGAAAA AGGGAATTCG AAGCGTGGCC TGCCTGAGTC CAGCCCCTGT 60 TCTTCTAGAA CCCGAGTTGT TCCAGACATA CTTGAAGGGT TTCCAAGAAC TGACTTAATC 120 CTCATTGGTG ACATGAGCCA TACTGCAAGT GCTTGGTGGC CCCATGGGGC TCATGGCTAC 180 CGTTCTGGGC AGCTCGGAGC ATGGGGCCTG CTCCTGGCCA GGCCATTGGG CTCCTGTAGG 240 GCATTTCCAC CAGAGTCCTC CAAATTCCAG AGGCTGTTCC CTGAGCTGCC TCTGCTGCTG 300 GGAAAGTGCT GCTGTCCTGG GAGACGGCTC CGGCTGCTGA CTTCCTGAGG CCCCAGCAAC 360 CTGGGGCTGG CTGAGGTCTG GTGGGGCCCC TGGGGGAGCT TGTCCTGCAC ATCCTATCCC 420 ACTGTCTACT CCCCTTTTCC TGGGAAATGT TTACATTCCA GACACTCAGC TATCTCTATC 480 CAGGGCTTCT CCAGGCTCTG CATTTTTCGC ATAGCTGAAC AGGGACCTGG GCTGGCCTGG 540 GGGCCGCTGC TGGGCCCTAT CTGTCCCCCT GGCTATCCCA TTTAGGTATG ACCATTTGCA 600 GGGCAGGCCC TGTTCCTAGC AAAGGCCAGG CCTGAGGCAC CCCCCGTCTC CCCCGACCTT 660 TTTGTCTCCA GGCATCCCCC AAAATAGGCA CTTGTTGGAG CTCTCCTCCC TGCCTGACCC 720 CAGCATGGGA TTCCTTGTGA GAGCCATTGG ACTAGACTGA CTGATGGGGG AGGCAGGTAG 780 CAATTGGGTT TGCTAAGCTA TCATTGCTAG ATCTCATCAG GGACTTCTCC TTTTCTGCTG 840 CTTTGAGGCC TGGCAGGGCT GCAAAGTAGG AAAGCCCAGG GCCTAAGGAG GCTGCCTCAT 900 TGTTGGGACC TTTTTCTGCA AGTCAGAGTC TCTGTGGTTG TTTTTTAAGT CTTTAAAGCA 960 ATCAGTTGAC ATAGCATCGC TTTGTGCTGT TCTCACCTAG CTCTGCAGGG TCACTATCCC 1020 CCGGGGTGGG AGGCGGGGGT CAGATTGGGG TAACTGATTA AGAAACTGAA CTAAAAACCT 1080 TCCTGAAGAT GGTTTATCAC TCTAAATTTG TAGTGGGTTT ATGTTCATAC CTTTCTTAAC 1140 CCACAATTCT ATCCCTGGGA CATCTGCCCC AGGAAATACT CAAGTGGTGC AGACAAAGAT 1200 AGGAGTCCAA GAATGCCATC GACATGGTTG TTGGATTGCA AACCCTCTAG CAACAAAGTA 1260 AATACTCAAC AATAAACCTC 1280
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