Tag | Content |
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EnhancerAtlas ID | HS010-01034 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr12:12162860-12163720 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYCN | MA0104.4 | chr12:12163357-12163369 | GGCCACGTGGCC | + | 7.22 | MYCN | MA0104.4 | chr12:12163357-12163369 | GGCCACGTGGCC | - | 7.22 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_19498 | chr12:12159217-12165094 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_39774 | chr12:12162828-12164867 | Jurkat | SE_49985 | chr12:12159945-12166471 | RPMI-8402 | SE_66709 | chr12:12162828-12164867 | Jurkat |
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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 |
GH12I012008 | chr12 | 12160347 | 12164912 |
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Enhancer Sequence | GGATTACAGG TGTGAGCTAC CGCACCCAGC CAAGAGATTG TTTAATCAGC AAAAGGCTGG 60 GCAGGGCAGT GGGGCCTAGG GCGGCACTTG CTATCAGATG TCTGGAGGGC AGGGTTGGCT 120 TTGGCCATAG ATGGACCTCG GTTCAAATCC TGGCTGGCCA TACCACTTAC CAGCTCTAGA 180 CCTAGAGCAG GTTAACATCA TGAATCTAAA CTACTTACCA CTTAACAAAG TGAGTGACTA 240 TCTATAACTG TTGCCGTTGT TACAAGAAAT CCACTTAGTA ACTGCACTGA AAGCCCCTCA 300 TCCCCAAAAG GCAAGAAATG GGGAACAACC GGGTGACTAA GGAAAACTGC AAGTGAAAGC 360 AGCTGTAATT TCTCTCGCTG TGGTTTGCGG TGCTCAACAC TCTTGCTTGG CTGGTTGTCT 420 TGGAGGGTTA ATGAGGTCTC TGCTGAGTGT CCTCAGCTTA GCAATGGGCA GTGGGGCTCT 480 GTTCACAGTC TCATCCCGGC CACGTGGCCT CCCGGGTTCA GACACCCTAG GCTGATGCTG 540 TGGTTCCATG TGCCTGAACA CGAGCATCCG AACTCATTTC CGGCCTGCCT GTCCCCCCAT 600 GCAACGGCTC CTGAAAAAGG GGAACCAAAT GCTGCCCATT TCACCCCCAT CAATAGCTGA 660 CAACGCCTGG GTTCCTGCTC TCCTGACATT CCCACTCATT GTCGTCAGTG GAGCGAGCAG 720 GCAGAGGGGA AGTGAGCTGC CTATCAGCCC CTGCAATCAG AAAAAGAGCC GGGTGCCTTT 780 AAGACGAAGG TGGTGGGCAG CCATCCATCT TCCCTAAACA CACACTCGCC TTGTTCTTCC 840 ATTTCTGGCT GAGTGATAAA 860
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