Tag | Content |
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EnhancerAtlas ID | HS182-14399 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr21:35894520-35895650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr21:35894791-35894805 | AAGGTCAAAGCTCA | + | 6.16 | Pou2f3 | MA0627.1 | chr21:35894724-35894740 | AATTATTTGCATAAAA | - | 6.16 | RREB1 | MA0073.1 | chr21:35895022-35895042 | TGGTGGGGGCGGGTTGGGGG | - | 6.17 | RREB1 | MA0073.1 | chr21:35895021-35895041 | GTGGTGGGGGCGGGTTGGGG | - | 6.43 | Rxra | MA0512.2 | chr21:35894791-35894805 | AAGGTCAAAGCTCA | + | 6.05 | TFAP2C | MA0524.2 | chr21:35895270-35895282 | TGCCCTGGGGCT | - | 6.11 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09811 | chr21:35888534-35895885 | CD14 | SE_26489 | chr21:35891955-35901947 | Duodenum_Smooth_Muscle | SE_29460 | chr21:35892837-35900438 | Fetal_Intestine_Large | SE_41006 | chr21:35893450-35895829 | Left_Ventricle |
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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 | AAGAAATAAG AATAAGGAAC AATAACCTAC GATCCTAGTT TGGTTTTAGA AATGCTGACC 60 AGTGATGAGA GGGCTGTCCA TAGAGCTCTT ACATCTCAAG CTGCGCGGTG TAGGTTTTCT 120 CTGCACTTCC AGATTGCCCT CCCCAAGTTT TCACAATGAA TATGCATTGT TTTACAAACA 180 GAAAAGGTCA GAGGAGTACT AAGTAATTAT TTGCATAAAA TCTTATCCCG TGCAGAAAGG 240 AGTGTACTCA CACAGGAAGG CCTAGGCACC CAAGGTCAAA GCTCAGCCTG TGCCTCCCAG 300 GGCAAAAAGG TCAGGGGTGG GGCGGGGATC CCAAATGCTT TATTTATACT TGAAGGGCCC 360 AGCAAGTTCG CTGTCCTCAC TTTGAGGAAG AAAAGACACT TTGGCTCTCT GGCGTGGTGT 420 CAGATGAGCT TCCTCCCACT GGGGGAGGCC TTTGGACAGG GTCCTCTCCC ATCCCAGCAA 480 GGTATGTGTG TATGTGTGTG TGTGGTGGGG GCGGGTTGGG GGGGTGCTCA GAGCCTGAGG 540 GGGACTTGCT TTACTGAGGA GCTGGCTGCA TTCTAGAAGC TCCTCTCTTC TTCCCTGACA 600 ATCTGTCAGC CCCTAAGGAC ATCAAATGGA ACTCTGGGAG CTGCCTTGAA GGTGGGTCAC 660 CTGTCCTAAG TTCCCCAGAG GAGGGTCAAA ATGGTAGTGG GCAGGAGAAA AGGCAAGCCC 720 AACCCCAGCT ACCCCTCTCC CTGCCGTGGG TGCCCTGGGG CTGGGAACCC TGCCAACCAG 780 AGGGTTTCTT AGCATCTGCG CCCAGTCTGG TTATCCCCTA TTTTCCTTTC AAGCCAGACC 840 TGGCAGTCCT GGGCTGATTT GCAGGCATCT TCTGCAGACT CCTGTTTCTC TGCTGAGTAC 900 CCCCAGCACC ACATGAGCAG GGAACCACTC TGGTCTGCTC AGTCTAGAGT GGGTCATGAG 960 CTCCAACCCT TGAGCAAATT CATGGAAACC TGCTGCGCAA ACCTTAGGGT GTTTGCATAG 1020 CCACGCCTAC CCCGCTGCAC CCTGCAAGCT CCCCAGTGAA CAGGGAAGGC TTTCTTTCCC 1080 CCATCATTAT CAACCCAGGA AGGTCAGGGG CAATGTCTGA GGTTGCTTTC 1130
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