Tag | Content |
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EnhancerAtlas ID | HS134-36798 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr22:38573710-38574620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr22:38574274-38574288 | CAATCGTAAACAAA | + | 6.51 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_27733 | chr22:38573617-38574602 | Fetal_Intestine | SE_28874 | chr22:38573421-38574950 | Fetal_Intestine_Large | SE_38157 | chr22:38567450-38578612 | HUVEC | SE_40165 | chr22:38573661-38574784 | K562 | SE_41851 | chr22:38573673-38574366 | LNCaP | SE_43287 | chr22:38570421-38574909 | Lung | SE_53822 | chr22:38573665-38574436 | Spleen | SE_64973 | chr22:38573811-38574478 | NHEK |
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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 | TCCGCCCACC TCCACCTCCC AAAGTGCTGG GGTTACAGGC ATGAGCCACT GCGCCCGGCC 60 GAATTGCCAC ATTTAACCCT CCAAACACCT GTAAGAAAAG GTCCAGGTCT CTCCACATTA 120 CACAGGAAAC TGGGGCACAG GTTACACAGT TTGCCAGGAT CTGAACCCAA TTAGGTGGAA 180 TCCAGAGCAT CAGGCTCTTA ATCCTCAAAC TGCCTTCAGG AGAAAGCTGA AAGAAGGTGG 240 CTGAGCGAGG CTTGCTCAAC AGGCTCTTAG ATTCCAAAAG CCAAGGCCCT CGTCTCAAAA 300 TGCACTGCTG CTCACGTGAG CCAGAGCAAA ACGTCCTTTC ACAAAAGGAA AAAGCATCTC 360 TTTCATTCAC TCCGCTTGGC TGGACCACAG CTGGAAGCAA ACTGCCCCGA AACTGTCACT 420 GGAGCTCCCA AGCACATGAG ACAGGGGTGA CTTTAAGAGA TCTTTGGGCT GGTGGCACGG 480 TACAGTGTGG CCCATGTTAT GACTCACTCC ACAAATATTT ACTGAGATGG ATTGTGGCAG 540 GCATTGTTCT AACCGCTGAG GATACAATCG TAAACAAAAC AGACTGGTCA GGCACGGCAG 600 TTCACTCCTG TAATCCCAGC ACTTTAGGAG GCCAAGGAAG GAGGATCACT TAAGCTCAGG 660 ACTTTGAGAC CAGCCTGGGT AATATAGTGA GACCTCACCT CTACAAAAAC TTAACAATTA 720 CCCAGGCATG GTATCTCTCA TGCCTGTAAG TCCCAGCTAC TAAGGTGGCT GAGGTGGGGG 780 GATTGCTTAA GTCTAGCAGG TCGAGGCTGC AGTGAGCTGT GATTGTGCCA CTGCAATCCA 840 GCCTGAGCGA CAGTGAGACC CTGTCTTAAA ACAAAACAAG GCCGGGCGCG GTGGCTCACA 900 CCAGTAATCC 910
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