Tag | Content |
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EnhancerAtlas ID | HS141-12188 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr21:44913990-44915000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr21:44914658-44914669 | AGTGACTCATC | + | 6.02 | JUND | MA0491.1 | chr21:44914658-44914669 | AGTGACTCATC | + | 6.32 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_27259 | chr21:44914115-44914869 | Esophagus | SE_33898 | chr21:44914068-44915114 | HCC1954 | SE_34698 | chr21:44912292-44916315 | HeLa | SE_35943 | chr21:44912749-44915484 | HMEC | SE_36970 | chr21:44912276-44928529 | HSMMtube | SE_51730 | chr21:44912852-44920634 | Skeletal_Muscle_Myoblast | SE_56062 | chr21:44912098-44916483 | u87 | SE_58009 | chr21:44913916-44914496 | VACO_9m | SE_63514 | chr21:44912763-44920801 | HSMM | SE_64394 | chr21:44913047-44915333 | NHEK | SE_67768 | chr21:44912098-44916483 | u87 |
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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: 2 | ID | Chromosome | Start | End |
GH21I043492 | chr21 | 44912519 | 44924893 | GH21I006043 | chr21 | 44913244 | 44915311 |
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Enhancer Sequence | GTCTCTCCCC CAACACAATC CCCCTGACCA AGACTTCCTG ACGTCCTGAG GGTGCGTCTG 60 CCTTCCAAGG CGAACATCTC ACACCAACTC TGCAGCCAGC AAGTTTGCGT TAGAAGCTGG 120 AAGCCTGCTG TTGGGGGAGC AGACCAGGAC TCCTCACACC CCAAGAGTGG CTGCTAGACA 180 CTCCCTAGCA TGCCCCGTGC CTGTCTGACC CCATGAAGCC TGACCCTGAT CGCCGAGTGT 240 GGCTGACTTT CTGAGCCCCT AAGGAAAAAC TCCAGAGTGA CCCTTAAACT TTGTAAAGGG 300 CAAAGAGGCC TGTGGGCGGA GACGGGGGAG GGGTTTCTGC TGGGTCCTGC CTGAACAGGT 360 CTGAGGCCAA AGGATCCCTA GGGCCGTCCT GGGTCAGAGT GAGGGGGGGC ACACAAGCCC 420 TCAGGACCCA CCAGGCGAGT CCAGGGAAGG CCCATGAAGG TGGCCACCGT GAGCCTTGTG 480 GTCCACAGGG CCAGGCTGGC ACATGCTGTG TTCTCACCCA GAAAGGCCGT TCCAGCTCCT 540 TCTGGACTCC TCCTCCTCCT CCCCAGTGTT CTCTGTCTCT CTGCCCACCC CGCTCTCTGT 600 CTCCCTCACA CACAGAGTAT AGAATTGTGG GGAGATGACT CTGTATTTCC TCATCGTGCA 660 TTTATCACAG TGACTCATCC ATCTGTGGCT GCTGGGTGAC TGGCAGGGTT TGCGTTGAGC 720 TTCCGAGTGA GGTTGATTCG GAAGAGGAAG GCATGACTGC CTGGCTATTA GCAGAATGTC 780 CGGCGTGGGC AGTGCCACCC AGCTGTCGAC ACTGACACCC AGGCAACCCT GACAGGTGGC 840 CACAGGGGGA TGTGTGTGTA CGCAGAGTTT CTCAGGACTC AACCTTCTTA AAAAGGAGGT 900 TTGCAGTGAA GAGCACAGGG GTACCCATCG GGAGAGGACG GAAATGCTTC CATCAACCCA 960 CTGGGTTTGG GGAACAAAGC AGAAGTGTGT TAGGGCAGGT GTCAGACCAC 1010
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