Tag | Content |
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EnhancerAtlas ID | HS105-24588 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr14:65193150-65194290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RELA | MA0107.1 | chr14:65193442-65193452 | GGGAATTTCC | + | 6.02 | ZEB1 | MA0103.3 | chr14:65194220-65194231 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_03251 | chr14:65192192-65193789 | Brain_Angular_Gyrus | SE_03953 | chr14:65190319-65195292 | Brain_Anterior_Caudate | SE_04856 | chr14:65180505-65197762 | Brain_Cingulate_Gyrus | SE_05821 | chr14:65180438-65199821 | Brain_Hippocampus_Middle | SE_06781 | chr14:65192065-65195493 | Brain_Hippocampus_Middle_150 | SE_07938 | chr14:65190169-65194504 | Brain_Inferior_Temporal_Lobe | SE_19856 | chr14:65188989-65195748 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20478 | chr14:65185982-65194236 | CD56 | SE_22874 | chr14:65186008-65194196 | CD8_primiary | SE_23289 | chr14:65190472-65194123 | Colon_Crypt_1 | SE_23289 | chr14:65194126-65197147 | Colon_Crypt_1 | SE_24426 | chr14:65191797-65193408 | Colon_Crypt_2 | SE_24426 | chr14:65193426-65194045 | Colon_Crypt_2 | SE_26750 | chr14:65181719-65194103 | Esophagus | SE_27717 | chr14:65189231-65195032 | Fetal_Intestine | SE_28783 | chr14:65190366-65194949 | Fetal_Intestine_Large | SE_32308 | chr14:65191832-65193491 | Gastric | SE_36148 | chr14:65181584-65194566 | HMEC | SE_47632 | chr14:65192885-65193854 | Pancreas | SE_50477 | chr14:65190429-65195289 | Sigmoid_Colon | SE_57093 | chr14:65190453-65193416 | VACO_400 | SE_57093 | chr14:65193490-65194055 | VACO_400 | SE_57603 | chr14:65191845-65193429 | VACO_503 | SE_57603 | chr14:65193483-65194199 | VACO_503 | SE_57932 | chr14:65193561-65193963 | VACO_9m | SE_64475 | chr14:65185799-65194369 | NHEK | SE_65298 | chr14:65181865-65199543 | Pancreatic_islets | SE_68953 | chr14:65192622-65194088 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH14I064714 | chr14 | 65180858 | 65194899 |
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Enhancer Sequence | AATGTGTACT CTGCAAAGTG GCATTGGTGA GCTCTAAGGG GTGGGCATGG GTGTTGCATG 60 GGTGTCCCTG TCCTTCCCAA AGGCTGCAGC CTGAAGTAGT CTGGCCACTC CACCCTTCCA 120 TCCCCCGGCT GCTCCAGGTG GGCCTGCCTG TGAGCCACAC CATCTGCTTT GGGAATAAAG 180 TCCACCTGAG GCTCTGTTTG CCTCACCTGG GTGCAGTTTA CTGCTTTCTC TGCTGCCCCC 240 GCCCAGCTGT GCCAAGGGGA GCTTACAGAG ACTCACTGAT GGCTTAGCCC TGGGGAATTT 300 CCTGGGGCCT GGGATGAGTC AGAGGCAGCC TGTACCAGGT GCTGGGGTGG GGCTGCGGAG 360 TCGGGGGATA ATGCTGGCTC AGCCAGTCAG TATCCAGAAA GTTTCAGGTT TGTGGTGAAG 420 CCGCCGGTGC CCCTGAGGTT TTGCAGTCTT AGGGAGAATA TTACCCCTGT TATGTGTCTT 480 GTCTTAACAT TGTAAGAACC AGATCTTTGC CCATCCCTGT ACAGTGACCC CAGCACAGGC 540 CACAGACAGG GGGGCACTTG GGAAGTTCTT CTTCACAACT GCCATTATTA TCACCATATT 600 GATGGTGTAT GGAGCACGTA CCCTATGCCA GGCATCATGC TCAGAGCTTT ACGAACAGCA 660 GGTGGCTTCA TCTGGGAGGA CACAGCCATG GGGTAGGCTG TATCCATCCT CATTTTACAG 720 GTGAGGAGCT GAGGCTCTGA GGGACTAAGT ACTGTGCCCC AGCAGTGGGG CTGGGCTGTG 780 AATTCCTTAG AGGGTACCTG GACCACTGTG CTGGCAGGTG GACTTGGGCA CCCTCATCAG 840 TGCTCATAGA GTCTGAGAAC AGGGCCCTTC TTGGGATTCA GTTTTGTTTT GTTAATTGTG 900 TTAAATGTAA ATACACATAA CATAAAATTT ACCATCTTCA CCATTTTAAG TGTACAGTTC 960 AGTGACAGTA GGTACATTCA TATCATTGTG CAATGTCATC ACTGTCTATC CACAGAACCT 1020 TTTCATCTTC TAAAACTGAA CTCTGGATGC ACTAAATAAT ACCTTCCCAC CCCACCTGCC 1080 CCCACCCCTG GCAACCGTCC CTCTGTTCTG TTTCTGTGGG CATTCAGAGG TTGACCCTTC 1140
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