Tag | Content |
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EnhancerAtlas ID | HS116-14153 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr17:1480380-1481540 |
Target genes | Number: 14 | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I001573 | chr17 | 1477152 | 1482396 |
|
Enhancer Sequence | AACTCCTGAC CTTGTGATCT GCCTGCCTCG GCCTCCCAAA GTTCTGGGAT TACAGGCGTG 60 AGCCACCGCG CCCGGCCCTG CTGGGTGGTT CTGCAAAGTG TTTCTCTTTG GACCAGCTCC 120 AGGCCCCAGA CTCTGGGGAG GGCCCACCCC ACTCAGCTGT GCCCAGGGCC TGTGGGTGTC 180 TGGCTGAGCC GAGTGGAAAG CGTGGTGCCA GCGGGGACCT GCGGTTTGGG AAACAGGCCC 240 AGAGAGGAGT GTGGAGGCTG GGCTTGGCTC TGCAGTGCCC TCGTCCAGAG AAGCATTGAG 300 TAATCGCGGA AACTCAGCAC CACAGATCCC GCCCCCCTCC CTCAGACCCT GCCAGGACAG 360 CCACAGCTTC CTCCAGGCCT GGGGAGGGGC AGGCGGAGGG CAAGCGGAGC TGGGATTACC 420 CCAGGGGCTG TTGCGGGAAT TGGGAGAGAG TTCCGGGCTA AATCTTAGCA CATGTCAGGC 480 TCTGCTGGCC CAGAGGTGGG AAAGGAATCC CAGCAACACA TGAGCTGGTC CCACATCAGA 540 GACTGTGGAT GATGATGTTT GAGTTTCAGT TTTTGGGTCA AGGCCTGAGC CAGAGAAGAA 600 GGAACCACTG TGGTTCCTTT TATGTTTCTG GGGCTTCTTG GAAAAAGATA CAGGTTTCAT 660 TTTAGCCAGG GCTGGAGAAA GCTATGGCCA GAGCTGGGCG CACTGAGGCT CTGGATGGGC 720 CCGTCTGGTG TATTCTGGAC TCAGTCACCC ATGTTGCTGC CCGTGATGAG GGCAACTGGA 780 ACTTCCGCAT TTAGCTTCAG GCAGCCAGAA CCTACCCATC CTTCCCAGTG AGCAGCCAGG 840 GCCAGCCCCA GGACTCGGCT GTAGTGGCCC CTGAGGCCAT AATGAGCTGC ACAGGTGCCT 900 GACCCTGGCT GGGGGAACTG ACTTCGTGTT GAATGCCAAG GCTTGTGAGC ACCCAACTGT 960 CTGCCCACTG ACCTGCTTCC CACGAGGTAT GGCCTTTCCC TGAAACACCC AGCAGAAACC 1020 CTGGTACCTG TCCCCTGAAG CAGGAAGATG AGCCCTTCTG GGACAGGCTG ACCCTGCCTC 1080 AGAGTCTCAG TCCCACCAGC AACCTCCCCC CGGCCATTCC CACACCCTCG CCCACCAGGC 1140 CACCTGCGGC TTCCAGGACT 1160
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