Tag | Content |
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EnhancerAtlas ID | HS003-38004 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr5:149901330-149904300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr5:149903217-149903228 | GGCCACACCCA | + | 6.62 | ZNF263 | MA0528.1 | chr5:149901872-149901893 | TGAGGAGAAAGAGGAGAATGA | + | 6.04 | ZNF263 | MA0528.1 | chr5:149902505-149902526 | AGAGGAGGAGCGGGAGATGGG | + | 6.38 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_00311 | chr5:149901586-149904308 | Adipose_Nuclei | SE_03211 | chr5:149901882-149904185 | Brain_Angular_Gyrus | SE_03966 | chr5:149901221-149907128 | Brain_Anterior_Caudate | SE_04872 | chr5:149894059-149907202 | Brain_Cingulate_Gyrus | SE_05832 | chr5:149875010-149907949 | Brain_Hippocampus_Middle | SE_06896 | chr5:149898215-149905271 | Brain_Hippocampus_Middle_150 | SE_07847 | chr5:149896704-149907730 | Brain_Inferior_Temporal_Lobe | SE_23236 | chr5:149901911-149904102 | Colon_Crypt_1 | SE_23910 | chr5:149902024-149902803 | Colon_Crypt_2 | SE_23910 | chr5:149902830-149903524 | Colon_Crypt_2 | SE_28046 | chr5:149901373-149903975 | Fetal_Intestine | SE_28971 | chr5:149901508-149903901 | Fetal_Intestine_Large | SE_31636 | chr5:149901707-149903571 | Gastric | SE_40767 | chr5:149900204-149907203 | Left_Ventricle | SE_42162 | chr5:149898635-149907280 | Lung | SE_45685 | chr5:149901281-149905428 | Osteoblasts | SE_47292 | chr5:149901848-149903800 | Panc1 | SE_47574 | chr5:149902053-149902774 | Pancreas | SE_48665 | chr5:149900269-149906911 | Right_Atrium | SE_50195 | chr5:149901233-149904114 | Sigmoid_Colon | SE_51701 | chr5:149901932-149903556 | Skeletal_Muscle_Myoblast | SE_52554 | chr5:149901525-149903652 | Small_Intestine | SE_53308 | chr5:149898538-149906728 | Spleen | SE_55717 | chr5:149902989-149903966 | u87 | SE_63488 | chr5:149901857-149904251 | HSMM | SE_65479 | chr5:149898594-149903853 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH05I150520 | chr5 | 149900147 | 149901471 | GH05I150521 | chr5 | 149901480 | 149903921 |
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Enhancer Sequence | TACACAAGAA GCAGGGTCCC CGAGCAGTTC AGAGCCCCCT CTGCAGCTCA GTGCCTGAAT 60 TCTCATTTGT GAAATAGGTG TAATGGTAGC ACCCGCCTCC TGGGGTTGTT GGGAGGGTTA 120 AATGAGTGAG TATATGTAAA GCACTGGGAG CATGCGGTGC CCACTGCCTG GCAAGTGCTT 180 TGTAAGTATT AGGGGAGCGT GCCAGGGGGA TCGCCTGCTG TGCGTGGGGT CCAGCACACA 240 GCAGGTGCTT GCCTAAAGGA GGCCACAGAG TAAGTGTGAA GTCAGAGGAG CATGCTCTGC 300 TAGGTGCCCC AAAATCTGTC AAGGCAATCT CCCCTAGGGA GGGCGTGTGC ACCCATTTTT 360 CAGATGAGCA AACCAAGGCT CCGGGTGTTA AGTTACTTAT GTGAGGTTTT GCAGCCTGTA 420 AGTGGAGAAG CCGAGATTTG AACCTAGACA TAGACAGTTT GGGCTCTCTA TCCCATGCTC 480 TTCCCTCTTG GTGGTGGTGG AGTATGGCGT TAATATACCT CCTGACCCAG AGCCATTTTG 540 CATGAGGAGA AAGAGGAGAA TGAAATCCCA CTGGCAGATG GGGAGCTGCT CTGGGCTTTA 600 TGGGGCTTCC AGAATGACCG CCGGGATTGG GGTCCTTGCA GGAAGGGTGT CCCAGAGAAT 660 CTGTCCTTGG CGGGGGGAGG TTGGGAATGG TGGGCGGGGG ATCCAGAGGC TGTGGTCAGA 720 GAAGTCTGAC CTGCAAGATG AAAGCAGACA CTAGCTGGGA CTCTTAGTTG GATGCTTTGG 780 AGGTGGCAGG GAATTTGTTC CTTCATTCAA CAAATATTTA CTGAGCACTC ACAGTGTTTG 840 TGGTCCTGTG CTAGCGGTGA TCGAAGTGGA CAAAGTCCCT GCTGTCATGG AGCTGGCATT 900 TCAGTGCTTT GGGAGTGGGT GGGTGACAGG CAGTGAGCAA ATAAACACAG GATGGGGCAG 960 GTGTGATCAG TACAAAAAGA AACAAAGCAG GGAAAGGACA CAGAGGGTAG TGGGGGTGGG 1020 AGCTTGACAT TATTTTAGGA AAGTCGTCTT TGATAAAGTG ACCTGAAATA AATGAGGGGA 1080 GGAGCCATGT GGCTTTCTGT GCAAAGAGTC TTCCAGGAAG AAGGGACGTT AAGTGCACGA 1140 GTCCTAAAGC AGCCTCTTGC TTGGTGTGAG CCAGGAGAGG AGGAGCGGGA GATGGGTCAG 1200 AAGTGGCCTG TGTCCGCTGC TGGGTGCCCG TTTGTGCCAG GCCTTCCTGG TGCACTTGCG 1260 CACTGGGCCC TGTCTCCTGG AGGGCTTCTC ATGGCGTGTT CTTTCACACC CTAATACAGC 1320 AGGAAGCTCT GCCACTGAAA GGTATTGTGA GCCAAGAATT TGAAGGCCCT TAGAAGTCCT 1380 GCAGTAGAGC AACCAGTGAG ATTTGTTCTC AACTGGCTTG ATCACAAAAC CCTTTCTTTT 1440 ACAGAGCACC CTCAGGGGAA CGCTGGCCTG GTTTATGGCT TTACAATGAC ATCAAGTCAG 1500 ATTATCTCCA TTGTCTGGTT GTCTCTTTTC TCTTGGACTC TGTACCCTTT CCTGCCATGA 1560 ACTTCGTTAA GTTCTATTCA GAGTCCCAGG CCTGAAAAGC GTCAAGAGGC TGACGTTTAT 1620 TGAGTGCTCA CTCAGTGCCA TGCACCGTCT ACATGCGTTG TGCAGATTCA CGCACTTCAC 1680 ACGAAGGCAG GTGGCTAGCA GCCTGATTTA AGATAGGAGG AAACTGAGGC AAAGGAGGAT 1740 AAGCAATGTG TCCAAGCCTA CGCCTCTGAT GAGTATAGGT CTGGGATTTG AACTCAAGCA 1800 GTCCGGCCCC AGAGGCCTTA GTCTTAACCA CGATGTGATG AGTCCAGGAG CCTCACATAC 1860 CACTTATTCA GGAGAAGTGA CATCAGAGGC CACACCCAGT GCACAGAGCT CCCACAGTCT 1920 TTGGGGACCA GGCGGTGGGC TGTGGCCATT GGGCGTAATT GGTACAATGG AGCTTGGGCG 1980 CTGTCTGGCC CCAATTCCTT GCTCTGCAGA AGGTAAACAG GAGGCCTAGG GAGGGGTGCG 2040 GGCATGTTCA GAGTCTCATC GTGGGGCCAG TGGTAATTCC AGGACTTGGT GCTCTTCCTA 2100 CCCTGTTGCC TAGGACAAGA CTATCCTTGG TTTTGAGCAG AGGCCTGTGA TTTTCTGCTC 2160 AAATGCATGC CCTCTGGTGG TCAAGGCACA TCTTTCCACT CTTTCTGCAA GACCAACTTC 2220 CCCGCTGTGT GCTGGGCTTG CCAAGTGGGG ATTGTCTGTG GGCTCCAGGG ATCTGAAAAC 2280 TCATTTTCCA GTTCCCACTG ATGCTGGATT CCCAGGGCAG TGTGAGAGCA GGGACTTAAA 2340 AGTCCAGACA GGTTCAAATC TCTCTGTCAT TTAGAAACAG AGTGACTTGG GTAAAATGCT 2400 CAACTCATCT GCAAAGTGGG GCTAATTACA GCTGCTGCCT CACTGGTCTG TGTTGAAAAC 2460 AAGACAGTGG GTGGGGAGCA CTGAGCCCAT TGCCTGGTAC CGGAGCCACT CAATAGATGG 2520 TAGCTATCGT GCTTTGTCAT CTCCAGGTTC AGTAAACAGC AGTGGTAGCA CTGTGTCCGT 2580 CTTGTGGCCC TGACCAATGT GTGCCCCTGT GAGATCCTGG AGGGTGGTGG GAATAGGGTC 2640 ATCCTCATCT GGATCCCTAC TTCCTGGCAC TGTCGTGCCT CAACCTTGAA ATTCCAGGTG 2700 ACCTGGGGCT AAACACACCC TGGCAGGGGT CTGGCAAGGA GTACCTGACC TCTTTCATTG 2760 AGCACTTACT GTGTCCCAGT CACTGAGCTC GGTGCTTTGC AGGCATTTCA TGGCTAATTC 2820 TCACAGCTAT CCTGTGAAGT AGGCACTTTA TTTTCAGATA AGGACCTGAG GTTCAAAAAG 2880 TTAAATGGCT TGTCCCGAAT GACATAGCTA CAGGTTGAGT GTCCCTTGTC TGAAATGCTG 2940 GGGACCGTAA GTGTCTCAGA TTTTGGAATG 2970
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