Tag | Content |
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EnhancerAtlas ID | HS080-23236 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr3:13058890-13061700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr3:13061369-13061379 | GCCCCGCCCC | + | 6.02 | PLAG1 | MA0163.1 | chr3:13060442-13060456 | CCCCCTAAGCCCCC | - | 6.54 | Znf423 | MA0116.1 | chr3:13060661-13060676 | TAAACCCTGGGGTGC | - | 6.11 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_00926 | chr3:13055265-13062149 | Adrenal_Gland | SE_04670 | chr3:13059250-13061061 | Brain_Anterior_Caudate | SE_08605 | chr3:13058267-13061047 | Brain_Inferior_Temporal_Lobe | SE_09375 | chr3:13049364-13059639 | CD14 | SE_10176 | chr3:13046655-13065411 | CD19_Primary | SE_10911 | chr3:13035699-13066171 | CD20 | SE_12494 | chr3:13059207-13059640 | CD34_adult | SE_12494 | chr3:13060064-13060458 | CD34_adult | SE_14626 | chr3:13048295-13060160 | CD4_Memory_Primary_7pool | SE_16175 | chr3:13054957-13059482 | CD4_Naive_Primary_7pool | SE_17506 | chr3:13048647-13059751 | CD4p_CD25-_CD45RAp_Naive | SE_17882 | chr3:13048254-13059646 | CD4p_CD25-_CD45ROp_Memory | SE_19986 | chr3:13042696-13060659 | CD56 | SE_19986 | chr3:13060706-13064930 | CD56 | SE_20899 | chr3:13048928-13059283 | CD8_Memory_7pool | SE_21767 | chr3:13050064-13059216 | CD8_Naive_7pool | SE_22360 | chr3:13049286-13059937 | CD8_primiary | SE_31302 | chr3:13059738-13060670 | Fetal_Thymus | SE_32598 | chr3:13049773-13064792 | GM12878 | SE_43204 | chr3:13058793-13061226 | Lung | SE_43685 | chr3:13049159-13061365 | MM1S | SE_50528 | chr3:13049434-13060971 | Sigmoid_Colon | SE_53233 | chr3:13049849-13059374 | Small_Intestine | SE_53444 | chr3:13049476-13061207 | Spleen | SE_58860 | chr3:13034529-13067396 | Ly3 | SE_61934 | chr3:13035948-13071595 | Toledo | SE_62359 | chr3:13034207-13065666 | Tonsil | SE_67345 | chr3:13049159-13061365 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 6 | Chromosome | Start | End |
chr3 | 13059077 | 13059166 | chr3 | 13059354 | 13060000 | chr3 | 13061201 | 13061436 | chr3 | 13059847 | 13059952 | chr3 | 13061400 | 13061601 | chr3 | 13061389 | 13061400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I013001 | chr3 | 13043330 | 13065896 |
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Enhancer Sequence | TGCTGATCAG CGGAAGAAAG CCTCTTCCCA TGTGTCAGAG TGGCTCATGC CCATGCCGCC 60 TTGCTGCTGG GCTCTGAGCT CTCGGCGACA AGTGCTGCCC TGTGGTGCTT GCCAAGAAGA 120 GCCTCACCCA CAACTCCGGT GAGGAAACCA GTAACGCAAA GCCTTGGACT CAGGTCCTCC 180 TCTGTGCTGT GGGACAGTGC TCCTCACAGG GTGGGCGCTA GCTGGCTGGA TGTGGGAATG 240 GATAGTTAGC ACCTGGCACA GTGTCAGGCA CAGAGTAGGT CTTCATCCCC TGAACGAAGA 300 CTCGATGCAG GGAGAGGGGG CGGCAGTCAC TAGCAGAGAT GGGAACCGAG GAGAGGGAGG 360 TGAGGCTGGC AGGGCTGAGG CAATGGTGAG GCCCACGGGT GAAAGGGGAA AGCAGCCATA 420 AGGGAATTTA TGTGTGCTCC AGGCAGTGCC CAGAGCCAGA GAAGTGGCGG CTCTGCTCTG 480 CTCTGCCCAG GACCTCCTGC CCATCCCAAA CTCAGCTCTG GGCTCTTCCC GGAGATAGAC 540 AGCACGAGCC AGGGTGTGTC CAGAAGGCGT GGGTGGGGAG GAGGCTGGTG ACCCCTTCCT 600 CAGCCTCAGG GAGTCCTGGT CTCTGCAGGC TGTCCAGAGC TGGGGAGCAG ATGGGTTGTG 660 AGGCTCAGAG GACAGGGCCA GGCCACTTCA GTGTGTGGGT GGGTGGCAGC GAGCACCGCA 720 GGAAGGATGG TGCCAGTTCC AAGTGGGAAC AAATGTCCTC GCGTCAGAGC TGCCTAGGCA 780 TGGCCCAGGC TGGGAGGTGG TGAGCACTCT GTCCCAAGAG GAACGCCCAC TGGCCCTCCT 840 GCAGAGGGGC ATCAGATGGC TAATTGTCCA GGAAGCTCCC TGGAAGCTCT CAAAGGCTGG 900 CTGCCAGCTG AGCTGTTCAC GGCCCTCCTG CCCAGATGCA GCCACGGTGG GAAGGCAGAG 960 GGGGGCAGGG CCAGGGCAGC CAAGGCCACC CCACTCCTTA TCAACCAGCA CCCTGGGCCC 1020 CATGTGTTCC AAGTGAGCTG CCCTGGCCCA CGAAGAGGCT CAAACGCCCC ATTGGCTCTC 1080 AAGGCACAAA ACGATCTTTC TTTTTCAATA TAATGCCAGA TGCAAAAGTG ATCTTCCTGC 1140 CTGACCTGAG AGGGGCTGTG GATTTATCAG GGCACTGCCC TGTACCCAGA GCAAGGCCTT 1200 TGTCTGCCAG GGGCCCAGAG GTGAGTGCCC AGAGAAAGGC CAGCCAGGGA AGACGCAGGG 1260 AGGGGAGGGG CGGGGAGCTG GTTAAAGGGT CTCATCCACC CTCCAGAACT ACTGTATCCC 1320 CACACGCATC TCACAGGCGG GGAAACAGGG GCTCAGGGAG GCTGCCTGTT ATACAAACAG 1380 CCAATGCCTC AGCAGCACCT ACTGCAGCTG GGGGAAGCTT ACAGGCATTG TCTCATGGAA 1440 GCTTCAGAAC GTCTCTAAGA GTCACGTCCA CGGTAGGAAG GGGCTGAGCC CAGTTTTGAA 1500 CTCAGGTCAG CCTGATTTCT GAGCCTGTGT GCTTCCCACT TCATCACGTT ATCCCCCTAA 1560 GCCCCCACGC TGAGACTCAG AGGACAAGGA GGGGGTGCCA CAGCCATGCA CCCTGCTGGA 1620 TGCCAAGCCA ACAGAACCCA GTGATGACCT GCCAAGAAGC CCGCCCAGCT GGCATGGCTC 1680 CCCCCCAACT CTACAGGCGA GGAAACAAGC CCAGAGAGGT TTAGCAACTT GCCCGAGGGC 1740 TGCACATCTC ACAACCTACC GTTGTGGGCT CTAAACCCTG GGGTGCCCAG CTCCCAAGCT 1800 GTTCTGTCCA GGATACAGCC TGCAGCCAGG ATCGTCCCTC TCAGAGTCCT CGGGCCAAAG 1860 TTCCAGAGAC CCTTCTCCCG GCTCCTTGAC TGCGGTCGCC AAACCCCTGG GCAGAGGGCC 1920 AGGGCTGGCA GGCGCACAGC TGCTCCACAC ACACCTCTCG CTTTTCCAGA TGTGAATGGG 1980 ACCCAGCCAG GGGCAACAGG CTCACTCGGA GGGGAATCTG AAGACGCAAG TGGAAAACTA 2040 TGCGCTGTCC GATCGCAACC CTCCAATCTG TCCCTGTGGC CGCCGGCAGC TCCGCCTTGG 2100 GCCACAGACC TGCTGACTCA GGGCTTCCCT GGCAGCCGAG GGGGCTGGGA TCCGCAGAGG 2160 GCCTGCTCCT GGCTGGCTGG CTGGTTGGGG CGTGGCCTTA GTCCTTTCAG GGGCTCTCAA 2220 CAGAATGGGG TAGGGGTCGG GAGGGCAGAG TGCTTCTCTT GGAGCCCAAG GCCCATCCTC 2280 CCCAGTTAAC CACAGGGGCG CCTGGCAGTT ATGGGTGCTA AGAGTGGGTT TGGGACAAAC 2340 CCAGTGCCAA TTATGGTGCC CACACCCACC CCACCACTCT CCTCTCATTG GTGGTGAGGA 2400 GGCCACCCGC CAGTGCTCGT GACACCCCTG TGAAGCTACC TGTCTATCAC CACTTGACAG 2460 CCACAAAGCC TCCCGTAAGG CCCCGCCCCA CAGCCCCGTC AGGTGGCCGT GCCATTCAAT 2520 GAGGAGACTG AGGCACAGAG AGGCCAGTCT GCCAGGCTCT GTGAGGCGGT GCTGCTTCTC 2580 CTACAGACCA TGTGGGCAAA CGGCAGCCAA GAGGGAGCGA GCGAATCACC CTTGGACAGG 2640 GCACAGCGGG CCTCCCAGTG CCGAGCCCTC TGCATTCTGT CAACAAGCCC TGAGGTTTCC 2700 AAAGTGCCAA TACCTGGAAA CCTTGGGACA GAAGGGGACT CAGGAAAATC CAGCTGTGGT 2760 CACAAGGAAA AGCACACGGA GAGCTCACCA AAGTCCAGGA CTCACCCGCT 2810
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