Tag | Content |
---|
EnhancerAtlas ID | HS145-16259 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr22:47130100-47133070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr22:47132290-47132300 | GCTAATTGGG | - | 6.02 | FOXC1 | MA0032.2 | chr22:47130644-47130655 | ATATTTACATA | - | 6.62 | Foxa2 | MA0047.2 | chr22:47130464-47130476 | TGTTTACACAGG | + | 6.14 | RREB1 | MA0073.1 | chr22:47130966-47130986 | CCCCCCAACACACACACACA | + | 6.69 | RREB1 | MA0073.1 | chr22:47130968-47130988 | CCCCAACACACACACACACA | + | 7.29 | SOX10 | MA0442.2 | chr22:47131413-47131424 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr22:47131413-47131423 | AAAACAAAGG | - | 6.02 |
|
| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_09349 | chr22:47130192-47135971 | CD14 | SE_14697 | chr22:47130289-47135628 | CD4_Memory_Primary_7pool | SE_17674 | chr22:47129977-47136955 | CD4p_CD25-_CD45RAp_Naive | SE_17901 | chr22:47129479-47137350 | CD4p_CD25-_CD45ROp_Memory | SE_18695 | chr22:47129530-47134167 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19505 | chr22:47129264-47136199 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20325 | chr22:47129975-47135578 | CD56 | SE_23520 | chr22:47130719-47132305 | Colon_Crypt_1 | SE_24287 | chr22:47130679-47131949 | Colon_Crypt_2 | SE_27442 | chr22:47130654-47136087 | Esophagus | SE_28432 | chr22:47129751-47141198 | Fetal_Intestine | SE_29215 | chr22:47129758-47141281 | Fetal_Intestine_Large | SE_31641 | chr22:47129922-47130667 | Gastric | SE_31641 | chr22:47130718-47135958 | Gastric | SE_38281 | chr22:47129860-47135670 | HUVEC | SE_40789 | chr22:47129770-47139213 | Left_Ventricle | SE_42260 | chr22:47130597-47139109 | Lung | SE_48916 | chr22:47130614-47133016 | Right_Atrium | SE_49561 | chr22:47130813-47132963 | Right_Ventricle | SE_50233 | chr22:47130014-47135867 | Sigmoid_Colon | SE_51682 | chr22:47130699-47137805 | Skeletal_Muscle | SE_52427 | chr22:47129806-47136051 | Small_Intestine | SE_53517 | chr22:47130708-47132392 | Spleen | SE_53517 | chr22:47132592-47135794 | Spleen | SE_58383 | chr22:47122081-47199614 | Ly1 | SE_62483 | chr22:47129710-47188820 | Tonsil | SE_65427 | chr22:47130748-47133722 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTGTCCAGA AGCCCATCAG CAGGTGAACG GATACACTAG TGCACCCACA CAATGCAATA 60 TGACTTAGTA ACCAGAAAGA AGGAACTGCT GACATGATGA ATCTTAAAAA AAACAAAATG 120 AGATAAAGCA GCCGGGCACA AAGACGTGCA CATGGCATGA TTCCATTTAC ATGAGATAAA 180 GCAGCCGGGC ACAAAGACGT GCACATGGCA TGATTCCATT TACATGAGAT AAAGCAGCCG 240 GGCACAAAGA CGTGCACATG GCATGATTCC ATTTACATGA AACTCTATTA GCATCGTGCC 300 TGTCCCTGGT GAGAAAACAG CCCAGGGCCC AGGAGAAGGT GCTGGGCTGC TGCGATCCGG 360 GTGATGTTTA CACAGGTGCA CACAATTATC AAAATTTAAC CAACTATGTG CCTTAAAATG 420 TCTGAGTTTT ATTGCATGCA ATTTAGACCT TGATAAAATC GATTTTTAAA AATCATGTCT 480 TAGGAGAGGA ATTAGTAGCG TGGAAAACAC TCTGCAGTAT GTTTTCTCAG CTTTTCTTTC 540 ATGCATATTT ACATATACAC AAATACCAAA TATTAATCAC GTCTAAGTCG AAGAGTGACT 600 TTTTGTGTAT GCTTTTCTGT GTTTTCTCGA TATTATTAAA TCAACATGAC TTACTTTTGT 660 AAGCAGGAAA AACATTTTTT TAAAGTATCT GTGGCATGCC TATGTTTTGC CAGGCACTTT 720 GCAGGGTGTG CTGAGGACAC GCTTTATAAA CACAGTACTG ACCTGCCCAA CGAGTTCACC 780 ACCAGCCTGG GACATCCCAA GTGGGGTTGG TGGAAGGAAG GGGAGGATCC TCCCACAAAG 840 GTAGAGCCTG GGCAGTAGTC CCCTCACCCC CCAACACACA CACACACACA CACACACTCT 900 TCCCATTCCC AACTCTAAAG GAATAAATGC AGGGTTTGTC TAAGTGTGTT TTGCGACAGT 960 CAGGGGAAAT AACCCAGATA TCAACTCAGT GTTTCCAGTT CAACGAGCAT GACCCACTTC 1020 AAGTTCCTGT TTTCGTCCTG CCCTACTTCC CACCAGGCTG GCGGCCCAGG GCACTTGCTG 1080 TCGCGGCTTC CTCAGGTGCA GACCTCACCC AGGCCCAGGA AGCTGCAGCG ATCCAAATTG 1140 CTAGTCCTTG TCTGTGCTCT TGTACAGTCA GTCACTGTCC CAGCATGATG ACCCACTGAC 1200 GAAAGTGCAC GTGCCTGGGT TCAAAGCCAG CTCCCTCTGT ACATCACTGC CTCTGGGCCC 1260 AGTCAATTCC CACTCCTACT GTCCACATCT GAAATAGGGG TGATGCTACG GAGAAAACAA 1320 AGGAGTCGGA ATAACTAAGC GGCCACCCCA GCAGGGCACA CACAGTGGCC TTGGCTTTGT 1380 CTTTAGCCCA TTGGTCACCT GGAGCTCCAG GGCTGCTCCT GCCTCATCTC ACAGGTCCTC 1440 CTAGGGCCAG TTTTTGCACA ATTCTCCACC TCTCATCATT CCTCAACCTA ATCAATCCCA 1500 GTGTGCCCAG ATACACCTGG GGGAATGGGG AGGGCTGGGC AATGCCACCT TGCTGACCAA 1560 ATTAAATGTC CTGTGAGCTG GTTCACATTC TTCTGCCCTA CTATGGCCCT ACTGACCTCA 1620 AGCATAGAAG AATCGAACCT GGGCCTGATT CCTTTTGGGG ACTGTAAAGC TATGAGAAAA 1680 AAACTAGAGA CAGTGTGGCT GTATTCCTGA ACTCATTCAC AACTTAGCGT TTCCCAACTT 1740 GTTGATGTTT TCCCATTGCA TGGGAGAGCA CTCCTGGGTG GAGAGGGCAG GCTGCTTCCT 1800 GGAGGAAGCC CACCAGCCAG GGCCACCAGC CAGGGCCCCA CCATCCATGG CCCCACAAAC 1860 CAGGGCCCTC CCTCTCCAAG AGGGACCAAG CTCCTGGCAG GCCAGTCAGG CAGCTCAGGA 1920 TGAACCCGCA CAAAAGCACC TTGGCTTAGC AAGAGTGAAG CAATTAGCAT GCCAAGAGGC 1980 AAACCCCAGC AGGCTGGACA AAAGCAGACG CCACACCACA CCAAGCCCTG ACCTGGGGGA 2040 CCAGAAACCA TAATGGGAGC TGGCTGGGGA CGCCAAGGCA GAAAGCAGTG ATGACTGACC 2100 TCCCACACAG ATGCCCTGTA AGGGTCTGGC GTCTCTGCGG CGGCTGGAGC CTGAGGGAAG 2160 CCTTACAGCC CAGTGGCTAC AAGCACAGCA GCTAATTGGG CCAGTCACTT CCAGCCCCTG 2220 CAGATCGGCC CCTGCATCCC TAGGACGGGA GCAGCTGCCT CTCAGGAACC CATCCGGTTT 2280 GAAGCCCAGT GGCCCGCACT TAGGAAGTGC TTGGGGGAGG CAGTCATCTT CCTGAAGCCT 2340 AGGGATTTAC AACAAAGTAC AAACCCTTCG GGCCCAGGTC AGGCACCTGT TCTCCTTGTG 2400 TGTGGGCCCT GGTGGGTGAT ATTTGGGGTG TGACATTTCT ACCAAAGGGG ACATGAGAAA 2460 TACCTTAGGA AAGTCAAGTC TCAGATGCCC AGCCACAGAT AGGTGACCCC AGGGCTGGAA 2520 ACCAAGTGTT GGTCATGGGT CTGAGACCAC CCCTCGACCT TGGCCCCACC TAACGTTCAA 2580 CTCTGTCCCC ACCAGAACCC AACCCACAGA TCCTCACCAC TCAGCACCAG AAAGCGCCCA 2640 GAAGAACTCC TGACCTCGAC TGCCCACAGG GTCTAAAGGT GTCATCCCAG GCTCCGAATA 2700 TCCACCAGAG AATCTTGGCC TCCGCCACAC CCACCCCATT CCAGCTCCGC ACATCCAGCA 2760 TGAATCCTGG CCTCTGCCAC ACCCACCCCA ATAATTAAAA AGAAAAAAGG CTGGGTGCGG 2820 TTGCTCACAC CTGTAATCCC AGCACTTTGA GAGGCTGAGG TGGGCAGATC ACCTGAGGTC 2880 AGGAATTCAA GACCAGCCTG GCCAACATGG TGAAACCCTG TCTCTACTAA AATACAAAAA 2940 TTAGCCGGGC GTAGTAGCGG GCTCCTGTAA 2970
|