Tag | Content |
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EnhancerAtlas ID | HS100-00098 |
Organism | Homo sapiens |
Tissue/cell | HT1080 |
Coordinate | chr14:55569400-55571220 |
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 | CAAGAATCGG CTAAAGTTTT CCCATTTAGT AAGAGTAGTA ATTAAGACAT ACACCTTCCC 60 TAAGCAATTC CTTTTCAAAA AGGAGCACAC ATTTAAAGAT AACTCATTAA TATCTCTTCT 120 GAGGCTGTTT ATCCAGTTTT GTCATGGCTC TAGAGCACAG GAATCTTTTT TTCTCCTCCA 180 TCTCTTTTTT AGCCAGTCTC TGAGAATCTC TGAGTTGCTA AGTATTATTT ATTTCTTCCA 240 TTTTACCCCC AGGAGCTTAG CCATTTTTGA TTTTTTGGCT TCGTTTTTTG AGCAACTTGA 300 ATGTCCCACA CATCAAAGGC CAATTAGCTA AAAGACAGGC TTCTTCACAC AACCCCTAGT 360 TGATATCAAC CTGTCTTTTT CTCAAAGCAA CAGGAAGCCA GGTGGCCAGC TCTAAAACCA 420 ATCCCACCAC ATAACGTTTT TCCTAACCTC TGACTTACAC CTCCGGGTTA TGCCTGGTTA 480 ACCTTCTCGT TTTCCTCCTG GGGCCAAGAG TGAGCTGCTG AGGAGTGAAA CAGACAAAGA 540 TTCACGTTCC TCTCCGGCCG CCTATGGGGA GCAGTTTCCA AACTCCCATC CCGGATCACG 600 CAGGGGCGGG GCAGTGCTAG CCTGGGGAGC ACCTGGCCGA CATGACTGAA GAGGCCCTGC 660 CCCAGAAAGG CCTCAAAAAC ACTCGTTAAA GCTAGGGCTG AGTCATCTGG GTGTGGAGGC 720 TGTCGGGTCA CATTCTTGAA ACATAACAGG CAAACAGGAC AGGCAGAGAA CATCTAGACT 780 GTGGATTCTG TAAAGCTTTT TCAAGGCCAG TTCACAGAAG CATTCCCTAC TCTGTGAGCG 840 TGAAATATAA AGGTGAATGC AGCCCCAGTG CCAGCACATA AGGCCAGTCA GTGCTATACA 900 GGGTCAGCTT AGCCCTGGGC TGACCCTTAA GATCAGGAAA AAGTTATGGG GCAGTGACTT 960 CTCAGCAAGT CTTTTCCATG TTTCTGGTGT CTTCGAATTC CTAGCTGAAC AGAATTTATC 1020 AAAGCAGAAG GTAGCTGTTT ATACCCCAGT TTACCCAGGC AAAGAGAAAT GCTTTGGAAT 1080 TGAGATATTT TCAGGGCATG AGTGGTTTAG ATCTCTGAAA CTGGAAGACG AAAATCCAGG 1140 TTATTAGAGA TCAGCAGCAC CTGAGAGGCA GGCTTCCTGG CACCTGAAGA CTCACAGACA 1200 AGCCTTGGTA GCCTGGCTTG TTTTCCTTGC AGTTCAAAAC CATTTCTTTG AGGTCATGAT 1260 CTGAAAGGGG ACACTGGACC CTGAGACCTA AATTCTGGTC CCTATGAGTA AATGCTTCAG 1320 ACAGATCAAG TTGGGGAGCT TCCACTGAAA AACACTGAGA CTAACACCCT GGTGTGACAG 1380 CCACACCTGT CTCCAAAGTG TACACACCAC CCCACCAGGA CATCACCAAC CTGACATTTA 1440 ATTAGCAATG AGACACTTGT TTTCACTCCT GTGGTCAAAG AATGGGGAAA TAGATGCTTT 1500 CTGTCTCCTT GCCTTTGGTT ATTTTTCTCC TACTTCCTGA GCTGGGCTGG GAGCAACAGA 1560 AAAGAGAAGG AAGGAGAAAC CCAGCAAGGC AAGAGCAGCT CCTTCCCTTC TTTGACACAT 1620 TTATGTTCTG CTCCTATAGT GGTGGAAGCA GGAAGTAGGG TGACTGGCCT GCTCCACTCA 1680 CATTCTGATC ATTTTCTCTA CAAGGCAAGG ATGGCTAGCA CCTCCAGTTG TGTGGAATGC 1740 TTCTATCAGG GGCCTGTGTA CGGTATCATT GACATCTGGA ATGTCTCATT CAAGCAATGA 1800 GGGCCACGTG TGGTTGTGGA 1820
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