Tag | Content |
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EnhancerAtlas ID | HS176-12662 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr14:65171420-65172940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr14:65171452-65171463 | TCTTATCTCCC | + | 6.62 | Stat4 | MA0518.1 | chr14:65172670-65172684 | TCCCTTCCTGGAAG | - | 6.06 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_01667 | chr14:65170138-65174210 | Aorta | SE_03251 | chr14:65171174-65173727 | Brain_Angular_Gyrus | SE_03953 | chr14:65167393-65177259 | Brain_Anterior_Caudate | SE_04856 | chr14:65167380-65178363 | Brain_Cingulate_Gyrus | SE_05821 | chr14:65167078-65178630 | Brain_Hippocampus_Middle | SE_06781 | chr14:65167470-65178320 | Brain_Hippocampus_Middle_150 | SE_07938 | chr14:65167829-65178149 | Brain_Inferior_Temporal_Lobe | SE_08852 | chr14:65171922-65172194 | Brain_Mid_Frontal_Lobe | SE_08852 | chr14:65172545-65173058 | Brain_Mid_Frontal_Lobe | SE_19856 | chr14:65169671-65177140 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20478 | chr14:65170052-65178236 | CD56 | SE_22874 | chr14:65171327-65178287 | CD8_primiary | SE_23289 | chr14:65169420-65174658 | Colon_Crypt_1 | SE_26750 | chr14:65169114-65176429 | Esophagus | SE_27717 | chr14:65169061-65176549 | Fetal_Intestine | SE_28783 | chr14:65169016-65176598 | Fetal_Intestine_Large | SE_32308 | chr14:65169312-65174204 | Gastric | SE_36148 | chr14:65168954-65176260 | HMEC | SE_49272 | chr14:65170129-65174244 | Right_Atrium | SE_50477 | chr14:65169120-65176913 | Sigmoid_Colon | SE_54434 | chr14:65170219-65177185 | Spleen | SE_57093 | chr14:65169032-65174194 | VACO_400 | SE_57603 | chr14:65169365-65174567 | VACO_503 | SE_57932 | chr14:65170543-65173862 | VACO_9m | SE_64475 | chr14:65169439-65176203 | NHEK | SE_65298 | chr14:65169344-65176523 | Pancreatic_islets | SE_68953 | chr14:65168090-65173064 | H9 |
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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 | CGGTGAGTGT CCCCTGATTC TCCTCTCTCC CCTCTTATCT CCCTGCATTA GGCTGAGCGG 60 CGGTGCCGGC AGTCACGCTG GGGCCCCAGT CCCTTCGCGG CCCCCGTGCC AGCCCCCTGC 120 GGGGTGAGGA CCGGGGCGAC CGAGGAGGGC CTGGAACTGT GTTGGCTGCT TCCCGGGCCA 180 CCCTGCCGCA GAGTGCGCGA GCGCAGGAGG GTCGTATGGG GAGACTTTTT CTGTCTTTTT 240 TTCCCTCCAC TCCGGAAACA AAAGGGGCAA ATGCGCCGGG CGGCTCCAGA GAGGCTCAGT 300 TTGAAATCCA GGAAGCCCGC GAGGCCGCGC GCGCCCGAGG GCTGGTGTTT GGCTGGAGCT 360 GTGGGCCTGG CGGGTGGACC CTTCTGCGCG AGGACCCGAG CCTCGGCTCC TGCCAGCCCC 420 GGAGGCGCCT GCAGCCTGTT CCGGGTTGGC GCCGCACGGT GCTCGCTGTT GGGAATCTCG 480 GCTACCTGTC CGGCAGGGAG GAGAGTGGGG GCCAGAAGCG GGGAGCGGAA AGCCCGGCCA 540 CCAGCTGCCT CGACCTCGTC CACTCCTGAA GTCGGTTTGG TTCTTCGCAC CCCTACACCC 600 AGCCCTTTGG TTTGGAAAGC CAGTATAAGG CGTGCAAGCT TAAATTTTTA AGGCGTTAAA 660 TAGCTACTTT GACTCTTCGG GGCGCCTTTG GAACACAAAA GGAAGAACGG AGGGGAGAAT 720 GGAATGGTTG GAGGCTGGAG AGGTGTGGCT TTTGGGGAGG GTGTTGTTAG AGGCCGCGAA 780 AGAGTTTGAT CCTCGAGGTC ACTCGCTAAT CTGTTGGCAT ATGTAGGTGC CTGTCCCCTG 840 CTCTGGGGGC CCCAGCAGGA GACCCACACT GCGTTCACCT TACGGGGAAC CCTGGAGTGG 900 GGGTTCCCAG AGTCTCCCCA GCCGTGCCTC TGCACGCAGC CCAGTCACAT GGCCCTTGCT 960 CAAGAAATAA TAAGCAGGGA GGGCAATGAC AGTCCGGAGC GGGGGAGGGC CTCCCCGTTG 1020 AGCACATCGG CCACCTCGCC TTCAGCAGTG TGGTTTTCCG GGCCATCCTT TGTTGGACAA 1080 GGATGGGATC CTGAGTGATT AAACCCCAGC TGTTCCCCAG GAGGAAACTA GGGAGTGAGA 1140 ACCAAAAGTG TACATTTATC TCTCTGTTAT ACATCTCTCC CCTGTGGTTC CGGGCTGGCC 1200 CCCTGGATGC AATGGCCTCA CTTCTCCTTT CGACACCTGC TGTCCTCCAC TCCCTTCCTG 1260 GAAGATAGGA CAACCCATTA GCTCCCTGGG TAACTTGCCC TGGGGATGGG GCAGGAAGTT 1320 GGGGGAAGAG GTACCCAGAG GCCAAGTCCT AGCTGCTGAG GGAGTGATTT GTTGAAGAGC 1380 TGCTTTGGGG GCTTTTCTAC TGCCTTTTAT TAGAAGTGGC ATGGCAGGGG AAGTGGAAAG 1440 AGCACTGGCC TGATAGTCCA GCACGGGTTT ATGCCTGAGT TTTAGACCTG GCTCTTCTGC 1500 ATAGCATGGA AGATTGGTAG 1520
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