Tag | Content |
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EnhancerAtlas ID | HS034-08958 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr14:55569580-55571360 |
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 | TCTCTTTTTT AGCCAGTCTC TGAGAATCTC TGAGTTGCTA AGTATTATTT ATTTCTTCCA 60 TTTTACCCCC AGGAGCTTAG CCATTTTTGA TTTTTTGGCT TCGTTTTTTG AGCAACTTGA 120 ATGTCCCACA CATCAAAGGC CAATTAGCTA AAAGACAGGC TTCTTCACAC AACCCCTAGT 180 TGATATCAAC CTGTCTTTTT CTCAAAGCAA CAGGAAGCCA GGTGGCCAGC TCTAAAACCA 240 ATCCCACCAC ATAACGTTTT TCCTAACCTC TGACTTACAC CTCCGGGTTA TGCCTGGTTA 300 ACCTTCTCGT TTTCCTCCTG GGGCCAAGAG TGAGCTGCTG AGGAGTGAAA CAGACAAAGA 360 TTCACGTTCC TCTCCGGCCG CCTATGGGGA GCAGTTTCCA AACTCCCATC CCGGATCACG 420 CAGGGGCGGG GCAGTGCTAG CCTGGGGAGC ACCTGGCCGA CATGACTGAA GAGGCCCTGC 480 CCCAGAAAGG CCTCAAAAAC ACTCGTTAAA GCTAGGGCTG AGTCATCTGG GTGTGGAGGC 540 TGTCGGGTCA CATTCTTGAA ACATAACAGG CAAACAGGAC AGGCAGAGAA CATCTAGACT 600 GTGGATTCTG TAAAGCTTTT TCAAGGCCAG TTCACAGAAG CATTCCCTAC TCTGTGAGCG 660 TGAAATATAA AGGTGAATGC AGCCCCAGTG CCAGCACATA AGGCCAGTCA GTGCTATACA 720 GGGTCAGCTT AGCCCTGGGC TGACCCTTAA GATCAGGAAA AAGTTATGGG GCAGTGACTT 780 CTCAGCAAGT CTTTTCCATG TTTCTGGTGT CTTCGAATTC CTAGCTGAAC AGAATTTATC 840 AAAGCAGAAG GTAGCTGTTT ATACCCCAGT TTACCCAGGC AAAGAGAAAT GCTTTGGAAT 900 TGAGATATTT TCAGGGCATG AGTGGTTTAG ATCTCTGAAA CTGGAAGACG AAAATCCAGG 960 TTATTAGAGA TCAGCAGCAC CTGAGAGGCA GGCTTCCTGG CACCTGAAGA CTCACAGACA 1020 AGCCTTGGTA GCCTGGCTTG TTTTCCTTGC AGTTCAAAAC CATTTCTTTG AGGTCATGAT 1080 CTGAAAGGGG ACACTGGACC CTGAGACCTA AATTCTGGTC CCTATGAGTA AATGCTTCAG 1140 ACAGATCAAG TTGGGGAGCT TCCACTGAAA AACACTGAGA CTAACACCCT GGTGTGACAG 1200 CCACACCTGT CTCCAAAGTG TACACACCAC CCCACCAGGA CATCACCAAC CTGACATTTA 1260 ATTAGCAATG AGACACTTGT TTTCACTCCT GTGGTCAAAG AATGGGGAAA TAGATGCTTT 1320 CTGTCTCCTT GCCTTTGGTT ATTTTTCTCC TACTTCCTGA GCTGGGCTGG GAGCAACAGA 1380 AAAGAGAAGG AAGGAGAAAC CCAGCAAGGC AAGAGCAGCT CCTTCCCTTC TTTGACACAT 1440 TTATGTTCTG CTCCTATAGT GGTGGAAGCA GGAAGTAGGG TGACTGGCCT GCTCCACTCA 1500 CATTCTGATC ATTTTCTCTA CAAGGCAAGG ATGGCTAGCA CCTCCAGTTG TGTGGAATGC 1560 TTCTATCAGG GGCCTGTGTA CGGTATCATT GACATCTGGA ATGTCTCATT CAAGCAATGA 1620 GGGCCACGTG TGGTTGTGGA TGGTGAGATA AAAATTCATC TTTGCCTCTG GAAAAACAGT 1680 CAGAAGGCAT GCCTTCCTGA AGGCGGGCAT ATCCTCTCTA AATCCAGCAT ATTGTATAGC 1740 ATTATGGAAT AGAGCAGAAA AGAAACCTAA CATTTGGCTG 1780
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