Tag | Content |
---|
EnhancerAtlas ID | HS045-24613 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr16:11676020-11678680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr16:11676566-11676577 | TGTAAACAAGA | - | 6.02 | NFAT5 | MA0606.1 | chr16:11678357-11678367 | ATTTTCCATT | + | 6.02 | NFAT5 | MA0606.1 | chr16:11677162-11677172 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr16:11678357-11678367 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr16:11677162-11677172 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr16:11678357-11678367 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr16:11677162-11677172 | AATGGAAAAT | - | 6.02 | PBX1 | MA0070.1 | chr16:11677943-11677955 | ACATCAATCAAA | + | 6.74 |
|
| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_06484 | chr16:11676726-11682216 | Brain_Hippocampus_Middle | SE_10082 | chr16:11677318-11681763 | CD14 | SE_12239 | chr16:11675986-11676712 | CD3 | SE_12239 | chr16:11677498-11680678 | CD3 | SE_16694 | chr16:11676900-11681847 | CD4_Naive_Primary_8pool | SE_17577 | chr16:11674393-11682049 | CD4p_CD25-_CD45RAp_Naive | SE_20221 | chr16:11674005-11681984 | CD56 | SE_21793 | chr16:11676268-11681680 | CD8_Naive_7pool | SE_22079 | chr16:11675384-11682101 | CD8_Naive_8pool | SE_22505 | chr16:11674007-11682149 | CD8_primiary | SE_23656 | chr16:11676998-11677458 | Colon_Crypt_1 | SE_23656 | chr16:11677521-11681613 | Colon_Crypt_1 | SE_27070 | chr16:11677599-11678943 | Esophagus | SE_31920 | chr16:11676792-11677461 | Gastric | SE_31920 | chr16:11677490-11679159 | Gastric | SE_42648 | chr16:11677535-11681909 | Lung | SE_50207 | chr16:11676201-11681943 | Sigmoid_Colon | SE_52871 | chr16:11677473-11678967 | Small_Intestine | SE_53430 | chr16:11676241-11682106 | Spleen | SE_61608 | chr16:11668804-11735966 | Toledo | SE_62803 | chr16:11650953-11682137 | Tonsil |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr16 | 11676086 | 11676659 | chr16 | 11676997 | 11677310 | chr16 | 11676200 | 11676316 | chr16 | 11677764 | 11678427 |
|
Enhancer Sequence | ACTGGAGACA TATAAGAAAA TATCACTCTT TATCCCATAA ATGTGTATGA TTATTATGTG 60 TCAACTAAAA ATAAAAGAGA AAATGGTCAA TGGCTTTTTA AAGGGTTTGA AAACAAGAGC 120 AAGATATAGT GAAATATCTA TTTCACTCAC AACGGAAAAA AAAAAAAAAA AAAAGAACTC 180 CCCACAAAGC TTTAGCCACA TGTGGGTGGT AAACTCTTCT AAAAATATAT CCTCAAGCTG 240 TGTATAGAAC TGTTTTCTAC ATTTGGGTAT CAGATCAACA CATAAAAGGG CAAGGCCTTC 300 AGAAAGATAA AGCGGCTTTT TAACTACCAA CTTAATCCTC GAAGATCGAT TCTTCCAGGA 360 AGAAAAAGGA GAAATATTCA ATTCTACTCT GGTCTCCATC TCCCAGCCCC CAGAAAAGAA 420 ACACTAAGCT AGGCCCATGA ATATGTATAT CGCAGAAATG ACCCCAGAAT AAAAAAAGGG 480 ATTCCTTAGG CAAAAGAAGG GCACTCACAT GCAAATTGTC AGGTCCCCTA AGAAAATAGC 540 CTAGTTTGTA AACAAGAAAG AGAACCAGCT GCGAGGGTCA AAAAGGTCTG GTCTTTTAGG 600 GTCTCTGGAG AAAAACGTTA TTTCCAATAA TGGGAGCACA GTGGATCCTG ACTATAATCA 660 ACTTTCAGGA ACTATCCAAA TTGTACACTT ATTAAATTGA ATATTGCTTA AAATTCTTAA 720 ACTAAGGAGG GTCACCTGGC AGGTTTTAAG CTACAATAAT TCTGCAATAC GGTTTTTGTT 780 GTCATGGAAT TTAACCTGTC TATCATTCCT GAAAATGTTC AAGGTGAATG GTGCGTCTTA 840 AGCCATAAAT GGTTAAGCAG GAAGGTAGAC AAAAGGGGAA ACCCGGACCT CCAGCTCTTT 900 GGGAAAGGAA GCGAGAAATT GGCCTTTGGT TATTTGATCC CAAACAAATT CCAGTTTCAG 960 TAGACCTCAG TAAAAGTACA GAAGCTCAGA GTGAAATATT TCAGAGAAAT GTGTGCCAAT 1020 TCCATCTTCT GAGTTCAGGC TGTTTCTGCA GGGCGGTATG TCCCACAAGT CAAAGATAAA 1080 GTTACCACAA TCTTAAAGCC AGGTTCAAGC ATGGCGTAAT GACAAATCAC AGTGATTTGT 1140 GGAATGGAAA ATGCTTCCAT CGGGGAGTTG GGCTGCTCCC CCACAATCAG AGTGGGCAGT 1200 TTTCCTCTGG ACTCCTGGTG AAACCACATC CCTAGTTTCC ACGTGAATCA CAGTTTTTCA 1260 TCAAACAGTG CAAGGAGATC ATTAATAAGA CTGAGACTGC ATTAGGATAC AAAATTGTAT 1320 GAACGCTGAT GACAATTTCA TAGAAAACAG GCACAAAGAC AAAAGACAGA AGCCGCCCGA 1380 TAAGGACAGC CAGTGGTAGT TGTTTCGTTC TATAAGATTA TGCCTTTCTT CTTTATCTTC 1440 CACACTTTAA TATTTTTTAA TAAAAAATTT CAAACTATCA GTGCATCATC TAGGAATAAC 1500 CTCATGGATT CAAGTTTAAG GCAAGACATC ATTAAGCTCT TAAACTTACC TGAGGCACAC 1560 TGTCAATTAA ATCTAAGGCT CCATGAGCTA AATAGCTTAA ATTCTCCAAC ATTATTTTCT 1620 CTGAAGCCTC CAGCTTTGGA TCCTGGTATA TAAACTCCTA CCTACTGCGA GGTGAGCAGA 1680 GAATTACCAT CACATAGACA CCCTCCAGAA TGGTTCCTTT CTTGTGTCCA TGCCTTAAGC 1740 TCTATGAAAT TACACAATTC TTCTACTGAA ATAACCTGCA GCCAAGGGAC AACTTCATTA 1800 GCTACAAAGC TGTTGTCACC TGTGTCCAGA GTGTCAATCA ATACAGGCTC AAACAACAAG 1860 ATGAAATTAT GAGGACCCTG GAAAATGCCA CTTGACCTCA AATAACAATT CTTAGGCAAG 1920 TAAACATCAA TCAAATTCAG AACAGACCAT GGGTGGCCAA ACAGACCCGG GAGACGTCAA 1980 AAATATGTGT GCTAAAGAAA CACAGAACTA AGGAAGTCTA TTTACCTGAT AGACCGCCTC 2040 ACCCACGGGG CTATTTTCAC TGCTGTAAAA GCGAAAACAA ATAGAGGACA AGTCACAGTG 2100 CCAAGAATAC AGGACTTCCT CTTGCAGATC CTCTTTTTTC CACCCTCACT GTAGCTCTGG 2160 GGAAATTCCT ATTCAGTGGG AGAAGTTTAA GTCACAAAAC GGCACCAGCC CATTCTCAAA 2220 GTGCTATTAT ACACCTCTGA GCAGTGAGGA TGGGTAATGT CAGCAAAATA TGCACTGTTT 2280 ATTTTCTTGA AAATTAACTT GGGCTGGAAA CGCCTTCCAG CTCCTTCCTC TCAGTGGATT 2340 TTCCATTTAC TGTCTTCAAC CACCTGGGCT TGTCTGTACC TCTTCCACAG CTCTACTGAG 2400 ACCCTCCTGT TTGTCTGAAC TATGTCCTCA TGTTCCTTCT GCCACATGTG CTCAGGCCTC 2460 AGTTTTTCCA TGAAACTTTC TCTAACTTAG CTGCCTCCTT TCCACTGTTC TCAAGCCCTT 2520 TCTGGAGTTA CAAGGGCATT AGCAAGCACC AGCTTTTTCG CCGGTGTGTG TTTCTACTTT 2580 CTACCCATTG CGTAAACCCC TCAGGACCAG GAGCCATTCT TCTGCATCCT TTACACGGCA 2640 AGGGTAGCGC TTTATTTCTC 2660
|