Tag | Content |
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EnhancerAtlas ID | HS184-09937 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr14:55569630-55571300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr14:55570002-55570012 | GGGGCGGGGC | - | 6.02 | LBX2 | MA0699.1 | chr14:55569718-55569728 | GCCAATTAGC | + | 6.02 | TBXT | MA0009.2 | chr14:55570761-55570777 | TAACACCCTGGTGTGA | - | 6.2 | TBXT | MA0009.2 | chr14:55570761-55570777 | TAACACCCTGGTGTGA | + | 6.41 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00244 | chr14:55563236-55576350 | Adipose_Nuclei | SE_00820 | chr14:55569710-55569933 | Adipose_Tissue | SE_00820 | chr14:55570220-55570627 | Adipose_Tissue | SE_02600 | chr14:55568405-55571441 | Astrocytes | SE_09388 | chr14:55568067-55576360 | CD14 | SE_23110 | chr14:55569439-55572086 | Colon_Crypt_1 | SE_23790 | chr14:55569549-55571705 | Colon_Crypt_2 | SE_24786 | chr14:55568610-55571711 | Colon_Crypt_3 | SE_26013 | chr14:55568329-55572045 | Duodenum_Smooth_Muscle | SE_26711 | chr14:55567642-55572310 | Esophagus | SE_27630 | chr14:55568256-55572821 | Fetal_Intestine | SE_28543 | chr14:55567548-55572997 | Fetal_Intestine_Large | SE_31668 | chr14:55569464-55571780 | Gastric | SE_33558 | chr14:55567245-55572042 | H2171 | SE_34039 | chr14:55568374-55571928 | HCC1954 | SE_34802 | chr14:55567662-55571944 | HeLa | SE_36310 | chr14:55568260-55572008 | HMEC | SE_37768 | chr14:55568071-55572110 | HSMMtube | SE_41170 | chr14:55568268-55571740 | Left_Ventricle | SE_42472 | chr14:55567635-55571940 | Lung | SE_44570 | chr14:55568270-55571944 | NHDF-Ad | SE_45117 | chr14:55568080-55571960 | NHLF | SE_46036 | chr14:55568077-55571810 | Osteoblasts | SE_46880 | chr14:55569583-55571299 | Ovary | SE_49010 | chr14:55569384-55571714 | Right_Atrium | SE_50181 | chr14:55568296-55571959 | Sigmoid_Colon | SE_52430 | chr14:55568292-55571855 | Small_Intestine | SE_56717 | chr14:55568352-55571704 | u87 | SE_57551 | chr14:55569509-55570126 | VACO_503 | SE_57551 | chr14:55570182-55571719 | VACO_503 | SE_64542 | chr14:55568330-55571772 | NHEK | SE_66903 | chr14:55567245-55572042 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 55570845 | 55571098 | chr14 | 55569733 | 55570176 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I055097 | chr14 | 55563775 | 55576469 |
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Enhancer Sequence | ATTTCTTCCA TTTTACCCCC AGGAGCTTAG CCATTTTTGA TTTTTTGGCT TCGTTTTTTG 60 AGCAACTTGA ATGTCCCACA CATCAAAGGC CAATTAGCTA AAAGACAGGC TTCTTCACAC 120 AACCCCTAGT TGATATCAAC CTGTCTTTTT CTCAAAGCAA CAGGAAGCCA GGTGGCCAGC 180 TCTAAAACCA ATCCCACCAC ATAACGTTTT TCCTAACCTC TGACTTACAC CTCCGGGTTA 240 TGCCTGGTTA ACCTTCTCGT TTTCCTCCTG GGGCCAAGAG TGAGCTGCTG AGGAGTGAAA 300 CAGACAAAGA TTCACGTTCC TCTCCGGCCG CCTATGGGGA GCAGTTTCCA AACTCCCATC 360 CCGGATCACG CAGGGGCGGG GCAGTGCTAG CCTGGGGAGC ACCTGGCCGA CATGACTGAA 420 GAGGCCCTGC CCCAGAAAGG CCTCAAAAAC ACTCGTTAAA GCTAGGGCTG AGTCATCTGG 480 GTGTGGAGGC TGTCGGGTCA CATTCTTGAA ACATAACAGG CAAACAGGAC AGGCAGAGAA 540 CATCTAGACT GTGGATTCTG TAAAGCTTTT TCAAGGCCAG TTCACAGAAG CATTCCCTAC 600 TCTGTGAGCG TGAAATATAA AGGTGAATGC AGCCCCAGTG CCAGCACATA AGGCCAGTCA 660 GTGCTATACA GGGTCAGCTT AGCCCTGGGC TGACCCTTAA GATCAGGAAA AAGTTATGGG 720 GCAGTGACTT CTCAGCAAGT CTTTTCCATG TTTCTGGTGT CTTCGAATTC CTAGCTGAAC 780 AGAATTTATC AAAGCAGAAG GTAGCTGTTT ATACCCCAGT TTACCCAGGC AAAGAGAAAT 840 GCTTTGGAAT TGAGATATTT TCAGGGCATG AGTGGTTTAG ATCTCTGAAA CTGGAAGACG 900 AAAATCCAGG TTATTAGAGA TCAGCAGCAC CTGAGAGGCA GGCTTCCTGG CACCTGAAGA 960 CTCACAGACA AGCCTTGGTA GCCTGGCTTG TTTTCCTTGC AGTTCAAAAC CATTTCTTTG 1020 AGGTCATGAT CTGAAAGGGG ACACTGGACC CTGAGACCTA AATTCTGGTC CCTATGAGTA 1080 AATGCTTCAG ACAGATCAAG TTGGGGAGCT TCCACTGAAA AACACTGAGA CTAACACCCT 1140 GGTGTGACAG CCACACCTGT CTCCAAAGTG TACACACCAC CCCACCAGGA CATCACCAAC 1200 CTGACATTTA ATTAGCAATG AGACACTTGT TTTCACTCCT GTGGTCAAAG AATGGGGAAA 1260 TAGATGCTTT CTGTCTCCTT GCCTTTGGTT ATTTTTCTCC TACTTCCTGA GCTGGGCTGG 1320 GAGCAACAGA AAAGAGAAGG AAGGAGAAAC CCAGCAAGGC AAGAGCAGCT CCTTCCCTTC 1380 TTTGACACAT TTATGTTCTG CTCCTATAGT GGTGGAAGCA GGAAGTAGGG TGACTGGCCT 1440 GCTCCACTCA CATTCTGATC ATTTTCTCTA CAAGGCAAGG ATGGCTAGCA CCTCCAGTTG 1500 TGTGGAATGC TTCTATCAGG GGCCTGTGTA CGGTATCATT GACATCTGGA ATGTCTCATT 1560 CAAGCAATGA GGGCCACGTG TGGTTGTGGA TGGTGAGATA AAAATTCATC TTTGCCTCTG 1620 GAAAAACAGT CAGAAGGCAT GCCTTCCTGA AGGCGGGCAT ATCCTCTCTA 1670
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