Tag | Content |
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EnhancerAtlas ID | HS177-16170 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr3:183271140-183271830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr3:183271768-183271789 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09997 | chr3:183268737-183274663 | CD14 | SE_11748 | chr3:183268653-183274978 | CD20 | SE_13968 | chr3:183270454-183275309 | CD34_Primary_RO01536 | SE_18732 | chr3:183269669-183275431 | CD4p_CD25-_Il17-_PMAstim_Th | SE_29421 | chr3:183269751-183272849 | Fetal_Intestine_Large | SE_43516 | chr3:183268800-183274916 | MM1S | SE_58323 | chr3:183220239-183279244 | Ly1 | SE_60504 | chr3:183222014-183274594 | DHL6 | SE_61518 | chr3:183220552-183274601 | Toledo | SE_62515 | chr3:183229386-183311073 | Tonsil | SE_67228 | chr3:183268800-183274916 | MM1S |
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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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Enhancer Sequence | AAACCCAAGA ACCAGAGAAG ACCAGTGATC AACTCGAGGG CACACAGCCA GCGGGCCTGG 60 TCCACAGCCA GGCCAACCCG CTAACAAAAC TGCTTCCAGG TATGCATTTT ATGATAGCAA 120 GGGATACAAA AGGATCAACC TAAATGTGCG TCCCCAGGGC ATTGAGCTAA CTTGACTTCA 180 CTCACTCCTG AGAGGGGCTG CAGTCAACGT GAAAGCACGT GATCAAGGTT GGTGGAGAAA 240 GTAATGTGTT TATATCAACC CATTTTGATG GCTGTGTTTA CACTTTATAT TTTACACACT 300 TCCCATGGAA TGAAGTCCCA GACCTAGTGG CAGCTTGCAT TGCAGTAACA AGGATTTCCA 360 GAACATACCC AGTCCCTGCT CCAGCAATGA CCAGATATAT AATGCTGAGT TTTCATTTCC 420 TCATCTGTGA AATATCAGCC ACCTTCATCA TGCTGTTACA AAAATAAAAT CAGATAACTA 480 TGTCTGTCTG GCACACAGCA GCCACTGCTT CCCTCAAACC CAGATATCCC CTTGTCTTAT 540 CAACACAGGA GACCTAATGA GTCCCACAGC AACCTGCTGA TCCTGCTCTA TGAATTACAA 600 AGAAACGTTT CCCCCCAAGC ACCTCAAAAA AAAAAAAAAG AAAGAAAGAA AACGCTTTCC 660 ATAATACTTT CATAGGTTAA TCGTTTTCAA 690
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