Tag | Content |
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EnhancerAtlas ID | HS117-02199 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr14:55569300-55571110 |
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 | TTTAAGTCTG CTTTTGTTAC AGCTCACTAA TAAATGGAGT GTATTTGCAT TTTTGCAAGG 60 AGGCCTGAAT TTTTAACACC TAATCATCTT TACCAAAGAG CAAGAATCGG CTAAAGTTTT 120 CCCATTTAGT AAGAGTAGTA ATTAAGACAT ACACCTTCCC TAAGCAATTC CTTTTCAAAA 180 AGGAGCACAC ATTTAAAGAT AACTCATTAA TATCTCTTCT GAGGCTGTTT ATCCAGTTTT 240 GTCATGGCTC TAGAGCACAG GAATCTTTTT TTCTCCTCCA TCTCTTTTTT AGCCAGTCTC 300 TGAGAATCTC TGAGTTGCTA AGTATTATTT ATTTCTTCCA TTTTACCCCC AGGAGCTTAG 360 CCATTTTTGA TTTTTTGGCT TCGTTTTTTG AGCAACTTGA ATGTCCCACA CATCAAAGGC 420 CAATTAGCTA AAAGACAGGC TTCTTCACAC AACCCCTAGT TGATATCAAC CTGTCTTTTT 480 CTCAAAGCAA CAGGAAGCCA GGTGGCCAGC TCTAAAACCA ATCCCACCAC ATAACGTTTT 540 TCCTAACCTC TGACTTACAC CTCCGGGTTA TGCCTGGTTA ACCTTCTCGT TTTCCTCCTG 600 GGGCCAAGAG TGAGCTGCTG AGGAGTGAAA CAGACAAAGA TTCACGTTCC TCTCCGGCCG 660 CCTATGGGGA GCAGTTTCCA AACTCCCATC CCGGATCACG CAGGGGCGGG GCAGTGCTAG 720 CCTGGGGAGC ACCTGGCCGA CATGACTGAA GAGGCCCTGC CCCAGAAAGG CCTCAAAAAC 780 ACTCGTTAAA GCTAGGGCTG AGTCATCTGG GTGTGGAGGC TGTCGGGTCA CATTCTTGAA 840 ACATAACAGG CAAACAGGAC AGGCAGAGAA CATCTAGACT GTGGATTCTG TAAAGCTTTT 900 TCAAGGCCAG TTCACAGAAG CATTCCCTAC TCTGTGAGCG TGAAATATAA AGGTGAATGC 960 AGCCCCAGTG CCAGCACATA AGGCCAGTCA GTGCTATACA GGGTCAGCTT AGCCCTGGGC 1020 TGACCCTTAA GATCAGGAAA AAGTTATGGG GCAGTGACTT CTCAGCAAGT CTTTTCCATG 1080 TTTCTGGTGT CTTCGAATTC CTAGCTGAAC AGAATTTATC AAAGCAGAAG GTAGCTGTTT 1140 ATACCCCAGT TTACCCAGGC AAAGAGAAAT GCTTTGGAAT TGAGATATTT TCAGGGCATG 1200 AGTGGTTTAG ATCTCTGAAA CTGGAAGACG AAAATCCAGG TTATTAGAGA TCAGCAGCAC 1260 CTGAGAGGCA GGCTTCCTGG CACCTGAAGA CTCACAGACA AGCCTTGGTA GCCTGGCTTG 1320 TTTTCCTTGC AGTTCAAAAC CATTTCTTTG AGGTCATGAT CTGAAAGGGG ACACTGGACC 1380 CTGAGACCTA AATTCTGGTC CCTATGAGTA AATGCTTCAG ACAGATCAAG TTGGGGAGCT 1440 TCCACTGAAA AACACTGAGA CTAACACCCT GGTGTGACAG CCACACCTGT CTCCAAAGTG 1500 TACACACCAC CCCACCAGGA CATCACCAAC CTGACATTTA ATTAGCAATG AGACACTTGT 1560 TTTCACTCCT GTGGTCAAAG AATGGGGAAA TAGATGCTTT CTGTCTCCTT GCCTTTGGTT 1620 ATTTTTCTCC TACTTCCTGA GCTGGGCTGG GAGCAACAGA AAAGAGAAGG AAGGAGAAAC 1680 CCAGCAAGGC AAGAGCAGCT CCTTCCCTTC TTTGACACAT TTATGTTCTG CTCCTATAGT 1740 GGTGGAAGCA GGAAGTAGGG TGACTGGCCT GCTCCACTCA CATTCTGATC ATTTTCTCTA 1800 CAAGGCAAGG 1810
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