Tag | Content |
---|
EnhancerAtlas ID | HS105-32455 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:1480370-1481540 |
Target genes | Number: 19 | Name | Ensembl ID |
|
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 |
|
| 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 |
|
| 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 | GCTGGTCTCA AACTCCTGAC CTTGTGATCT GCCTGCCTCG GCCTCCCAAA GTTCTGGGAT 60 TACAGGCGTG AGCCACCGCG CCCGGCCCTG CTGGGTGGTT CTGCAAAGTG TTTCTCTTTG 120 GACCAGCTCC AGGCCCCAGA CTCTGGGGAG GGCCCACCCC ACTCAGCTGT GCCCAGGGCC 180 TGTGGGTGTC TGGCTGAGCC GAGTGGAAAG CGTGGTGCCA GCGGGGACCT GCGGTTTGGG 240 AAACAGGCCC AGAGAGGAGT GTGGAGGCTG GGCTTGGCTC TGCAGTGCCC TCGTCCAGAG 300 AAGCATTGAG TAATCGCGGA AACTCAGCAC CACAGATCCC GCCCCCCTCC CTCAGACCCT 360 GCCAGGACAG CCACAGCTTC CTCCAGGCCT GGGGAGGGGC AGGCGGAGGG CAAGCGGAGC 420 TGGGATTACC CCAGGGGCTG TTGCGGGAAT TGGGAGAGAG TTCCGGGCTA AATCTTAGCA 480 CATGTCAGGC TCTGCTGGCC CAGAGGTGGG AAAGGAATCC CAGCAACACA TGAGCTGGTC 540 CCACATCAGA GACTGTGGAT GATGATGTTT GAGTTTCAGT TTTTGGGTCA AGGCCTGAGC 600 CAGAGAAGAA GGAACCACTG TGGTTCCTTT TATGTTTCTG GGGCTTCTTG GAAAAAGATA 660 CAGGTTTCAT TTTAGCCAGG GCTGGAGAAA GCTATGGCCA GAGCTGGGCG CACTGAGGCT 720 CTGGATGGGC CCGTCTGGTG TATTCTGGAC TCAGTCACCC ATGTTGCTGC CCGTGATGAG 780 GGCAACTGGA ACTTCCGCAT TTAGCTTCAG GCAGCCAGAA CCTACCCATC CTTCCCAGTG 840 AGCAGCCAGG GCCAGCCCCA GGACTCGGCT GTAGTGGCCC CTGAGGCCAT AATGAGCTGC 900 ACAGGTGCCT GACCCTGGCT GGGGGAACTG ACTTCGTGTT GAATGCCAAG GCTTGTGAGC 960 ACCCAACTGT CTGCCCACTG ACCTGCTTCC CACGAGGTAT GGCCTTTCCC TGAAACACCC 1020 AGCAGAAACC CTGGTACCTG TCCCCTGAAG CAGGAAGATG AGCCCTTCTG GGACAGGCTG 1080 ACCCTGCCTC AGAGTCTCAG TCCCACCAGC AACCTCCCCC CGGCCATTCC CACACCCTCG 1140 CCCACCAGGC CACCTGCGGC TTCCAGGACT 1170
|