Tag | Content |
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EnhancerAtlas ID | HS098-22901 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:1480340-1481540 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr17:1481439-1481454 | GGGACAGGCTGACCC | - | 6.32 | SPI1 | MA0080.4 | chr17:1481159-1481173 | AACTTCCGCATTTA | - | 6.42 | SPIB | MA0081.2 | chr17:1481159-1481171 | AACTTCCGCATT | - | 6.27 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_09501 | chr17:1477198-1482172 | CD14 | SE_24303 | chr17:1480428-1481001 | Colon_Crypt_2 | SE_24303 | chr17:1481005-1481629 | Colon_Crypt_2 | SE_25267 | chr17:1480380-1481766 | Colon_Crypt_3 | SE_27390 | chr17:1480364-1481857 | Esophagus | SE_41871 | chr17:1480390-1481757 | LNCaP | SE_50860 | chr17:1480343-1481848 | Sigmoid_Colon | SE_53184 | chr17:1480354-1481865 | Small_Intestine | SE_68949 | chr17:1480336-1481912 | 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 |
GH17I001573 | chr17 | 1477152 | 1482396 |
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Enhancer Sequence | GTAGAGACGG GGTTTCACTA CGTTGGCCAG GCTGGTCTCA AACTCCTGAC CTTGTGATCT 60 GCCTGCCTCG GCCTCCCAAA GTTCTGGGAT TACAGGCGTG AGCCACCGCG CCCGGCCCTG 120 CTGGGTGGTT CTGCAAAGTG TTTCTCTTTG GACCAGCTCC AGGCCCCAGA CTCTGGGGAG 180 GGCCCACCCC ACTCAGCTGT GCCCAGGGCC TGTGGGTGTC TGGCTGAGCC GAGTGGAAAG 240 CGTGGTGCCA GCGGGGACCT GCGGTTTGGG AAACAGGCCC AGAGAGGAGT GTGGAGGCTG 300 GGCTTGGCTC TGCAGTGCCC TCGTCCAGAG AAGCATTGAG TAATCGCGGA AACTCAGCAC 360 CACAGATCCC GCCCCCCTCC CTCAGACCCT GCCAGGACAG CCACAGCTTC CTCCAGGCCT 420 GGGGAGGGGC AGGCGGAGGG CAAGCGGAGC TGGGATTACC CCAGGGGCTG TTGCGGGAAT 480 TGGGAGAGAG TTCCGGGCTA AATCTTAGCA CATGTCAGGC TCTGCTGGCC CAGAGGTGGG 540 AAAGGAATCC CAGCAACACA TGAGCTGGTC CCACATCAGA GACTGTGGAT GATGATGTTT 600 GAGTTTCAGT TTTTGGGTCA AGGCCTGAGC CAGAGAAGAA GGAACCACTG TGGTTCCTTT 660 TATGTTTCTG GGGCTTCTTG GAAAAAGATA CAGGTTTCAT TTTAGCCAGG GCTGGAGAAA 720 GCTATGGCCA GAGCTGGGCG CACTGAGGCT CTGGATGGGC CCGTCTGGTG TATTCTGGAC 780 TCAGTCACCC ATGTTGCTGC CCGTGATGAG GGCAACTGGA ACTTCCGCAT TTAGCTTCAG 840 GCAGCCAGAA CCTACCCATC CTTCCCAGTG AGCAGCCAGG GCCAGCCCCA GGACTCGGCT 900 GTAGTGGCCC CTGAGGCCAT AATGAGCTGC ACAGGTGCCT GACCCTGGCT GGGGGAACTG 960 ACTTCGTGTT GAATGCCAAG GCTTGTGAGC ACCCAACTGT CTGCCCACTG ACCTGCTTCC 1020 CACGAGGTAT GGCCTTTCCC TGAAACACCC AGCAGAAACC CTGGTACCTG TCCCCTGAAG 1080 CAGGAAGATG AGCCCTTCTG GGACAGGCTG ACCCTGCCTC AGAGTCTCAG TCCCACCAGC 1140 AACCTCCCCC CGGCCATTCC CACACCCTCG CCCACCAGGC CACCTGCGGC TTCCAGGACT 1200
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