Tag | Content |
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EnhancerAtlas ID | HS182-17794 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:133889230-133892230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr5:133892129-133892149 | ACACACACCACACACACACC | + | 6.16 | RREB1 | MA0073.1 | chr5:133892118-133892138 | ACACAACACACACACACACC | + | 6.19 | RREB1 | MA0073.1 | chr5:133892158-133892178 | ACACAAAACACACCCCACAC | + | 6.25 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00886 | chr5:133885924-133892235 | Adrenal_Gland | SE_02152 | chr5:133889221-133892206 | Aorta | SE_06180 | chr5:133888998-133892479 | Brain_Hippocampus_Middle | SE_11045 | chr5:133874973-133893428 | CD20 | SE_13932 | chr5:133889292-133892302 | CD34_Primary_RO01536 | SE_15160 | chr5:133889603-133892484 | CD4_Memory_Primary_7pool | SE_17673 | chr5:133889315-133892597 | CD4p_CD25-_CD45RAp_Naive | SE_17966 | chr5:133888765-133893355 | CD4p_CD25-_CD45ROp_Memory | SE_18783 | chr5:133889081-133893006 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19361 | chr5:133889171-133892963 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22714 | chr5:133889285-133893012 | CD8_primiary | SE_38826 | chr5:133885812-133893016 | HUVEC | SE_40774 | chr5:133889191-133892419 | Left_Ventricle | SE_42303 | chr5:133889215-133892433 | Lung | SE_48716 | chr5:133889226-133892248 | Right_Atrium | SE_52569 | chr5:133889256-133892221 | Small_Intestine | SE_53502 | chr5:133889155-133892659 | Spleen | SE_58884 | chr5:133859047-133893050 | Ly3 | SE_59789 | chr5:133859380-133891828 | Ly4 | SE_61248 | chr5:133858888-133892472 | HBL1 | SE_62577 | chr5:133838672-133892328 | Tonsil | SE_65308 | chr5:133887260-133892327 | Pancreatic_islets | SE_68727 | chr5:133890107-133891233 | H9 | SE_68727 | chr5:133891468-133892239 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr5 | 133891162 | 133892151 | chr5 | 133890594 | 133890960 | chr5 | 133890161 | 133890536 | chr5 | 133891612 | 133892163 | chr5 | 133889963 | 133891123 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I134546 | chr5 | 133882688 | 133892810 |
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Enhancer Sequence | GTGGGGTTTC CCCATGTTAG CCAGGCTGGT CTCGAGCTCC TGACCTCATG ATCCGCCCTC 60 CTCGGCCTCC CAAAGTGCTG GGATTGCAGG CGTGAGCCAC TGCGCCCGGC CGTAAGCCAT 120 GCTTTTGACA TCTTGAACCT TTTACGGGAG TTCTTAGAGG GGGAGTCAAG TGCCTGGCAT 180 ACAGCAGATG TTCAGGAAGC CATTGCTATT ACCGGCCTCT GGGTAGGTTC CCCTGCCAGG 240 GCTGGTTCAG AGATGAGTCC TCTGGGCTTT ATACTCTTCT GGTCTCATGA GGCAGAGAGA 300 CCCCTGGCCG CTCTTGTCAG GAGGAGGCCA CATGGCCCTG GGTCTTGCCT CCAGCTACGG 360 AGTTCAGCCA AGTGCTTCTT TATGCAACCT GGGAAACCCT CCAAGTCATG TCTCAGGGCA 420 GAGGGGTCTT GTGTCCTGGC CTCCCCCACC CACCAGTCTG CCTGGTCTGG GCAGCTTGGG 480 GTTTTGGCTG TCTACTCCTG GCCTTGGCAA CCTTGTGGCT CTTGCTCGAT CCCATGTAGA 540 CCAGGCCTGG GGCAAAGATC ACAGCTGTTA CCTCCCCTGA CGTTGGCACC CTCATTTCGT 600 GGCAGCTGCA TCTGATTGGA TCATAGGCAC AGCAGACTCG AAGCCCCAAT AGGGTGATCT 660 GTGGGGATTG GAAGGGGAGG GGTCAGGCAA TCCTGTTCCA GTGACTCCTG ATGGCTGAGT 720 GTTTATTAAT ACTTGTCTGG GGTCTTCGGA GAATCAGGGG TGCCCCAGGC CTCTCCAGAA 780 GTGAGAATAT GCATGCCAGG TCACTGCCAC ACATACCAGT GCCTAGGGTG AAGGGGTGAA 840 GGTCAGGCCA CCAGGTGGGC ACAGCGAGGT CAGTCTTGAT TAGGCTTGGC CCAGCGGTCT 900 GTCCTCTCTA CTTGATGTCA GTGTCATTTG GTTCCGGAAA CATCTCCTGG CCTGGGTAAT 960 TAATTGCAGA TGTTTCCACA CCAGTAGCTT GGCTTCAGTC TGCCTGTAGG GTGCTTTATC 1020 TGTTGACATC AAGAGGAGGG CACGTGTTCC GGCTGCTTTG ACTTTACGAG GTGCATTCCC 1080 AGCATAGGCA TGGCTGTGCT AAGCTGACGT GAGCTGGGCA CTCCTGGCCT GTCCGTGATC 1140 TTTGGAGAGG ATGGACTGGG GGTGGGGAAG TGCTCCCTTA GAGACATCTC CACGCCTCTT 1200 CTGTTGCTAT CTCCCTCCGG CCCAGCCACT GCATCCTCCT GGCACCTCCC ACTGCACAGC 1260 CCTCATCTGG AAGGCTGCCT GGTAGCTGCC CGGGTCAGAA TTGTTAGAGA AACCCTGTTC 1320 TTGAGGACTT GCTATGCTGA GCCTGTGTTC ATCTTTTCAT TTAACAATCA TATTAGCTTT 1380 ACAAACTGCA TGTAACTGTC CCCATTTTAT AGATGAGGAA GTCGGGAAAT TCTGGGGAAT 1440 TCCCTGCATG GCCACCGGGG CCTAGTGGGC TGGGCCAGGA AATCAAAGGC CCCGAGAACA 1500 AGCCCTGGGC TGCCCCTGTG AGGCCCAGAG ACAGAGCCCT GTGCCCCCGT CATCCCAGCA 1560 TGCTGGTTCT GGCTGCCCTC CCCCAGCTGC CACCCCAGGC CCCCTCTGTC CCTCCCTCCC 1620 TGGCCTTTGG GTGGGTCTGC CCACCTCATG GTCTGAAATC TGTCTGAACA ATGAGCACTT 1680 GTCTCGCCCC TCTCCAGACT GAATTGAGTG AGGGCCTGTC CTGCCCCTCA CTGGGGCCAG 1740 AAGTCTCAGC CAGGGCAGAA CCCACCTCTG GTGTGTGTCT GGTCTTCTAG GGTAAAGACC 1800 CCCTCCCCTC CCATAGATCC CAGCCAGCTG ACGCCCTCCT CCCAGCTGAC CTCCGCCGTC 1860 CTGGCTACAG CTGAGGGTGA GGCCTTGGCC TAGGGTCAGG TCAGTCCATG CCTGGTAGGA 1920 GAGCTTCCTT CAGAGCCAGA GCCAGAAGGG GGCAAACAGA TGAAGAGGAG AGACCCAGGA 1980 AGGACAGCAG ATACCTTCTG ATTGTGAGTC CCTTCACCTT GGCTCTTCAG AAGGAGCACA 2040 GTGATCTTGA TCCCAAGAGG CTTGGCCAGG TGGCCGCTGA CCAGGCAAGC AGATGTGGGT 2100 AGTTATGCCA GGAAGTGGTG GGCATCCGGA CACCCCCACT CAGCATGTGC TTAGGGCACA 2160 ATCAAAGCTG GTTCACAACC AAATTACAGG CTGCATTTTT AAAAGAATGT GTTTGTTAAG 2220 TAACAGTTTC ATGGGGAAAG GCAGAATTGT GTTGGACCGA GTGTGTTAGT ATTGCTTCCA 2280 TATGGAATCA CCTGTTAGTG TGGGGTGTGG TCATACCCTG ATAATGACCT AGAACCTTCC 2340 TTCATGTGGG CCTCTTGTGT GGGAAAAGGT GGTGCCAAGC CCCTTCCCCT TCTCCGTGCC 2400 CCCTCGACCT TATATAGGCC TTCCTCCTGG CTCGGAGGCC ATTCTCTCTG CCGGGTTGGG 2460 CCCCTGCCTC CCCGTCTCCT TCATCCTTCC TGCCCTTTTT GCTGACATTG GGTGTGGTGA 2520 TGGGGAAGCC CAGGAGCCCT CGCCACAGCT CTGCCATGTC TCTGTGCCAT CTAAAGCCCT 2580 GCCCCTTCCT CCCTGTCAGC GCTGAGTCAC AGCTTCTGGC AGCCTTGCCC CCGACCCCAG 2640 GATGCCTCTC AAGTAAGGGG CCTCCCCGCC CTGGCAGAGC TGGCCAGATG GAGGCCAGGC 2700 TCCGAAGCAA TAACCATGGC AACCAGCGGG GGGTGGGAAG AGCTGGCTTT TTGAACTGGC 2760 ATCAGGAACT GAGGGGCAGC ACACAGCTGA GCCAAGGGGA AACCGTGCCC TCCTGAGGCA 2820 AAGTGCCCCC TATATTCCAT TTCAGGAGAG GGGTAACATC CCAAGGTCTC AACACACACA 2880 CACACATCAC ACAACACACA CACACACCAC ACACACACCT CACACATCAC ACAAAACACA 2940 CCCCACACAT ACCACATGCA CACACACACA CATCACACAA CACATACACA CACACCACAC 3000
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