Tag | Content |
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EnhancerAtlas ID | HS047-00420 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:19262530-19267120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:19264193-19264204 | AGTGACTCATC | + | 6.02 | JUND | MA0491.1 | chr1:19264193-19264204 | AGTGACTCATC | + | 6.32 | KLF14 | MA0740.1 | chr1:19265299-19265313 | GGCCACGCCCACCC | + | 6.69 | Klf12 | MA0742.1 | chr1:19265299-19265314 | GGCCACGCCCACCCC | + | 6.15 | SP3 | MA0746.2 | chr1:19265299-19265312 | GGCCACGCCCACC | + | 7.52 | SP8 | MA0747.1 | chr1:19265300-19265312 | GCCACGCCCACC | + | 6.62 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_01018 | chr1:19264421-19265533 | Adrenal_Gland | SE_01018 | chr1:19266482-19269122 | Adrenal_Gland | SE_04479 | chr1:19264572-19272928 | Brain_Anterior_Caudate | SE_05621 | chr1:19264299-19273049 | Brain_Cingulate_Gyrus | SE_05988 | chr1:19262507-19263769 | Brain_Hippocampus_Middle | SE_05988 | chr1:19264170-19284746 | Brain_Hippocampus_Middle | SE_07595 | chr1:19264656-19273075 | Brain_Hippocampus_Middle_150 | SE_08107 | chr1:19264273-19273098 | Brain_Inferior_Temporal_Lobe | SE_14542 | chr1:19264723-19267474 | CD4_Memory_Primary_7pool | SE_18508 | chr1:19263136-19264500 | CD4p_CD25-_Il17-_PMAstim_Th | SE_18508 | chr1:19265120-19266840 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19155 | chr1:19264047-19266523 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_26830 | chr1:19265382-19267058 | Esophagus | SE_30281 | chr1:19264828-19266052 | Fetal_Muscle | SE_33643 | chr1:19260296-19269410 | H2171 | SE_35893 | chr1:19262679-19269705 | HMEC | SE_37377 | chr1:19264472-19266650 | HSMMtube | SE_47330 | chr1:19263226-19269376 | Panc1 | SE_53460 | chr1:19264689-19266079 | Spleen | SE_64648 | chr1:19263135-19269243 | NHEK | SE_65885 | chr1:19263066-19266097 | Pancreatic_islets | SE_65885 | chr1:19266305-19267001 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 19263315 | 19263478 | chr1 | 19264931 | 19265239 | chr1 | 19264909 | 19265543 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I018936 | chr1 | 19262683 | 19270200 |
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Enhancer Sequence | GGGTCACAGC TGCAACTCCA GTGCCCAGCA CAGAGCCTGG CACATAGGAG GCCCCATAAA 60 TATTCACTGG ATTAAAAAGG CCCAGTAAGT GTCATCTCCA GGGCCTTCTC TAGGAGATCC 120 AATCTAGGCC AATGCAGCCC TGTCGCCTTA GATATGGCCA CCCTGCCAGC CCCTCCCTGC 180 CAGCCTCAGT TTCCCCAAAC AACCTCCACA GTCCAGGCCA ACTCTGCTAC TCTCTTCTCT 240 GCACCTTGAA GCCTGGGCCT ACCTTGCATG GAGCAGATGA TGGGAAAGTT GGTGTCCACG 300 GCTCTCCATC CCTGGGACAT TGTCTTTCTG CCTAGGCCTG GCCAAGCCCC CATGGACCCT 360 CCACCCCATC CCCATCCCGT GTCTGCTGGC TCTTGCTTAA GTGGAAGCCA GCAGGGGGTC 420 TGGGCAGCAG GTCTTTGGGC ACTCAGGTCA AGAGGCAGGA GGCCCAGGGG GTCTGTGCCC 480 AGGAGAGTGT GGGGGCCCCC AGGCCCAGGG TTATGTTTAC AGCTTTGAGA AAAACAGCAA 540 CTCCCAAGGC TATTTTGGAA ACCTAATATG TACTTTGGGT CTCTCCACTG TTTATTCCAA 600 GTGACTGTGC TGCCCTGGAG GTAAATGTAG GGCACCTCAG GGTAATCTCC CGCATACTTA 660 CTCACCCGCA GCCGCCCTGG AGCCAGCTGC CTGGGAGCCC AGATTTTCCT TATCATGTGC 720 AGCCTGAAAA AATGAGGGGC TGGCAGCCAG GCAGAGCCCA CCAGGCAAGA GTCAGCACAC 780 CTGGGTTGAA AGCAAGGCTC TGCGGCCTTA AGCCAAGTCA CTTCTCTAGG GCTCAGTCTC 840 CTCACCTGTA AAATGGGTGA GAATGACCCC ACCTGGATTC AATGAGGATG TGCAAACACA 900 AACTGGCTGC AGGTGGGGCA AAAAAAAAAA AAAAGCACAG AACACAGGAT CCTAGGACAT 960 CAGACGGGGA AGTCCAGGTC ATTCATAAAT GAGAAGTCTG AAGCTCAGAG GTGGGAGGTG 1020 ATATGTCCAA GGTCCCACAC AGGCAGCGGC TGGCTCAGTG CAACTCCAGA GACTAGGAGC 1080 TGCCTGCCAT GCCGCTGGTA AGGGGAGGAG AACATTCCAG AGCAATCTCC AGGAGGGAGG 1140 AGGGAAGAGT GACAAGGACC CAGCTAACAA AAGACACGTG GGGCTTGTGC AACCAAGGAT 1200 GGGTAACAGG GCAACGGTCA CCTGTCTGTG CAGAGCCGTC ATGGTCCTCA CTAGCTGGGA 1260 AGGGGCAGGT TCCAGCGCAG CTGAGGCAGG TAATTAGACT GCAAACACGC GCACCAAAAG 1320 AATTAGTGAC TAAATACAGC TCAAGGGGAT GGACTCATTA CTTAATCCCA GGCTCCTGTC 1380 ATCATGGCGG GCCCTGGCAT TCCACCTGAT GTGAACCACT GGGGAGTGTG GAGGCTGAGC 1440 ACCAGGCAAC CCCACAACAC ACAAACAAGA GTGTTCCTCC CAACTACCCA TGGGGCTGGA 1500 GAGAGAAGTC AGTCCCCTTA AGATGAGACG GGGAATGAAA TGGAGCAAAG CCTCCCAGGG 1560 ACCCTTCCAT GACTGCAAAG CCCCTCGGAG GGCATCTTTA TTGGAGCTTG TCATCTCCTC 1620 ACCCTCATTC TGCTGATGGG GAAAGTGAGG CTCACCAAGG TGCAGTGACT CATCCAGGGT 1680 CACATAATCA TAACAGCATT ATGGAGGCTC CCAACGGCCT GGCCCAGCCG CCACTGGAGG 1740 GCAGAGCCTT GGGGCTCTCA GATGGATGGA GGGTCCTCCG AGGGGAATCC CTCAAGCGCT 1800 GCCCAGATGC TGCCGAGCAC CCCACACATG GGATGCAGAG GGTCACTAGC CCCAGCTATG 1860 CAAAAGAACC GGCACCAGCA CAGCCTCTCT TCTCAACTCC AACCCAGCGG GGGCTCTCTT 1920 CCCCCTGAGA TTTGGGCCTC CAGCCACAGG ATTCCCAGCC CGGACTCAGC AAAAAGCCAA 1980 AAAGGAGATG GTCCAGGCCA GCATGGCGAG AAGAAGCCGG CTTGGGGCAA AGTGGGAGGC 2040 CACTTGCAGC CACCCCCTGT CCCTTATCCC AAAACACTTT GACGTCAGGC AGAGCTGGGA 2100 TGGGCGTCCA ACTCAGCCGC TCCGCAGCTG GTGATCTGCT AAAGCGACTT TACCTCTCTG 2160 AGCCTCAGTT TCCTCATCTG TAAAATGGGA ATAACAATAG TACCTACACC TCCCTGGATG 2220 GTGAAGACCC CATAAGATCA TAAACACCAG TGCCTAACAT TATTTTGCTC CTCCTAGTGA 2280 GCAAGCCCCA CCTCCAGCTG CTGGGAAGGC TGGGAGGGAG GCTACTGGGA GGGCTGCTAC 2340 AGCGTCCAGG GCCCCGGGCT TGGCTGAGCT GCACCATGCT TCCCCTTAGA GGCTCTGTCT 2400 CTGGGTTCCC TCTCCCATGC TGGGACTGGG GAACTGTCTG GTATCCAGAG TGACCAAGTG 2460 CCCAGCACAC CGTAGGCCCT CAACCGCTAC TGACTGGATG AATGAGCTTG TGAGCTGGAG 2520 CCACTGGGCG TAACCACCAG CAGGCCTCGG GGGAAGCCCA GCTCTGCCTG TGCTGACTTA 2580 CTGTGTGGCC TTGAGCCCAT CCCTGCACCT CTCTAGACCT TCTGCACAAG GAAGCTCCGA 2640 CCACACCAGG GACTGAGACT CCCCCACCTC ACACCTAGGG AGACCCTGCA GGGAGGGTGG 2700 CCAGAGGACA GCCTGCCCAG TGGGGAGCCC CTCCCAACTG GCCTGGCCCC CCCAGGGACA 2760 GACAGCAGGG GCCACGCCCA CCCCTGCAGG CCCTCAAAGG CAGTAGGCAG TCTCCTCCTG 2820 GTGATTTTGC CTTGGGACAG ATGGGACACA GTGTGGTATC TGTCAGGCCA GATGGCCTGG 2880 TTGGCCCCAG GGGCCGGGAC ACCAGCTGGG AGTCCAGCCC TGGCAGGCAA CACTGCTTAA 2940 CCCCTTCTTG CCCCAGCCAC AGGAGCTAGT GTCCCCCTGG CAACTTAATT ACTGGTGTAC 3000 ACTCAGGCCT CCTGTCCTCT CCCCTTGGAG GTGAGGGGCC TCCCTGGCAC CTCTAGGGCC 3060 AAAAGGGAGG CTGGGAGGCT GTGGGAGAGA GGAAGCCACA GGGTGGGTGG GAGCGGAGAA 3120 GATGCCACTG CTTGGCCCTG AGGGCAGCCC AGGACCGCCA GGAATCTGCC AACCCAGGGA 3180 ACCAGCAGGC AGGAGCACTG ATTCCAGGCC AGGGAGCCCT CTGGGGCCAC ATGGGGCTGG 3240 CTGTTCTGCT TCCAGGACAT CTGTCTGCGG CAGGGACCAC CAGGCCAGAG GCCACCGGCC 3300 ACCTTTATCA AGCCCCCTGC CCAAACCATA GAAACAGCAT TGCCACATGA AGGAGGACAC 3360 CCAACTCGGA CAGGCTGGCT GAATGGCTGT GGACATGTTG CTCAACCTCT CTGGGCCTCA 3420 GTTTCCCCAT CAGGAAAGAT GGGACCAGAG TGATCCCTGG GATTCAGGCC ACTTCTAGCT 3480 CAGAGGGCTC CCTGACTCCT AGAAAAGGAA TGTGCCTCCC TCCCAGAAAC TTGTGGGATA 3540 CTACAGGGAC CAGCCAGATC TTTTCTGCAT GAAGATTGTG TCTCAACTTG TATCTGAGTC 3600 AAGGCACAGT CTCTCAGGAA GTGGAGAAAA GGGAGATTGT AGGTGGGAAG AGGGTACGCA 3660 GCAAGGTAAT GGTGCTGCCT TGAGAACCAC CAGGCAATTG ATATCCAACC ACTTTCCTCC 3720 TCTGTGAAAG GCTAAACAAA GGGGGAAATG AAGCAGTAGG GATCATGGTT AGACACCAGG 3780 AAGCACTTCC CAATGGAAAA GGCCACAAGG ACACTGGACG GCCCGTCTCA GAAAGGGTTC 3840 TGGAATGTGC TTCCTAGGCA GTAAGATCTT CAGGCAGGAT TTGCAGTGGT CCTAGCCCCA 3900 AGATGAGGAA GAAACAGATG ACCTCTGGAG ACCCTTGGAG GAAAAGAAGC CAGTGTCCAG 3960 TAGGGTAAAG TAAACAGGGC CTTGGAGTCT CTCCCCTCAG GGGCTCAGCC AACCTGCTGT 4020 TCCAGATGCG GGAGGGTGTC ATCTCAGGGC AGAGCATAGC CAAGCTTGGC CCCAGTCTGG 4080 GGCCTGCATG CTGGTTCAGT AGACACCTCT AGAAGTCTCT CAGAACAGAG GCTGCCAGCA 4140 ACTCCCGAAA AGCCAAGAAC CCATGAAAAC AGCAGAGGAG GAAGAGCTAG GTAAGGGAGC 4200 TGCCGGCCAG GAGTGAGAGC TGTCTGTTGA CACAGCAGAG AAGCAGAAAC TTGGGGCTGG 4260 GACCTACAGA CCTGACTTTG AGCCCTAGCT CCGCCACTCG CCCCGTGCAA CTTTGGGCAA 4320 GTCACTGCCC CTCTCTGACA AAAGGGAGAG AAAATATCTA ACCAATCTCT AAGGACTCTT 4380 CCAGCCCTGA TTTAACAGTT CCTTGGCAAG CTCCCCAGAT TCTGCAAGCT CCCAGTTCAT 4440 GCAGCATCAT CCCCAAAGCC CAAGCATAGG GACTGAGCAC CGTGGCCCAG AAAAGGATGG 4500 ATGGATGGAC AGACTGATGG ACAAACGGAT GGATGGATGG ATGGATGGAT GGATGGATGG 4560 ATGGATGGAT GGACAGACGG ACGGACAGAC 4590
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