Tag | Content |
---|
EnhancerAtlas ID | HS182-17765 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:131788640-131790560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr5:131788832-131788853 | TTCTGCTTTCTTTTTCTTCTC | + | 6.11 | KLF4 | MA0039.3 | chr5:131790009-131790020 | GCAGGGTGTGG | - | 6.62 | REST | MA0138.2 | chr5:131789592-131789613 | TCCAGCACCATGGCCTGGTCA | + | 6 | ZNF263 | MA0528.1 | chr5:131788746-131788767 | TCCTCCTTCTTCTTCTTCTTC | - | 6.36 | ZNF263 | MA0528.1 | chr5:131788762-131788783 | TCTTCTTCCTCCTCCTCTTCC | - | 7.68 | ZNF263 | MA0528.1 | chr5:131788753-131788774 | TCTTCTTCTTCTTCTTCCTCC | - | 7.89 | ZNF263 | MA0528.1 | chr5:131788765-131788786 | TCTTCCTCCTCCTCTTCCTCT | - | 8.2 | ZNF263 | MA0528.1 | chr5:131788759-131788780 | TCTTCTTCTTCCTCCTCCTCT | - | 8.39 | ZNF263 | MA0528.1 | chr5:131788756-131788777 | TCTTCTTCTTCTTCCTCCTCC | - | 9.32 |
|
| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_09163 | chr5:131788117-131797621 | CD14 | SE_10915 | chr5:131787711-131797453 | CD20 | SE_11856 | chr5:131788689-131797117 | CD3 | SE_13479 | chr5:131789528-131790142 | CD34_Primary_RO01536 | SE_14495 | chr5:131789106-131797177 | CD4_Memory_Primary_7pool | SE_17370 | chr5:131789423-131795425 | CD4p_CD25-_CD45RAp_Naive | SE_17764 | chr5:131787920-131797394 | CD4p_CD25-_CD45ROp_Memory | SE_18258 | chr5:131787905-131797327 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19103 | chr5:131789195-131790583 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19972 | chr5:131788439-131797324 | CD56 | SE_22284 | chr5:131788012-131797561 | CD8_primiary | SE_25340 | chr5:131788298-131808279 | DND41 | SE_30917 | chr5:131789781-131790449 | Fetal_Thymus | SE_39368 | chr5:131788855-131790154 | Jurkat | SE_42103 | chr5:131789200-131790498 | Lung | SE_50051 | chr5:131788916-131790464 | Sigmoid_Colon | SE_52336 | chr5:131788917-131790452 | Small_Intestine | SE_53285 | chr5:131788823-131790516 | Spleen | SE_62219 | chr5:131721125-131837948 | Tonsil | SE_66244 | chr5:131788855-131790154 | Jurkat |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I132452 | chr5 | 131788089 | 131817782 |
|
Enhancer Sequence | TTGTCTTAAT AGTCTTCTAG TCTCTATTTT GTTTTTGTTT CTACCTGGAG GTGGCAGCGG 60 CGGTGGTGGC TGCTTCTTGT TGTTGTTGTT GTTGTCGTTG TCGTCATCCT CCTTCTTCTT 120 CTTCTTCTTC CTCCTCCTCT TCCTCTTGTT CTTCTTCTTC TTCCCTCTTC TTTCTTCCTT 180 CTTCCTTTTT CCTTCTGCTT TCTTTTTCTT CTCCCTCTCT CTGTCTCTCC ATCTCTCCTT 240 GTTGGAGGCT TTCCTTAAAT GCCAAATATC TCAGCTATCT GTTGGTATTT ATTAATGGAG 300 CAATAAAAGG CTGAACTAAA CTCTGCTTGG GGAGAATTTA TCAACTGGGG TTTCACTACA 360 GGAAGCAAGA CAGTCTTTTA GTTAACAAGC CTCCAATGAG CACCTTTTCT CTAGAGCTAG 420 GTTTCTTAAC CTTGGTACTA GTGACATGTT GGGCCAAAGA ATTCCTTGTT GTCAGAGGCT 480 GTCTCATGCA TTGTAGAATG TTTAGCAGCA CCAGTGACTT CTGCCTACTA AATGCCAGTA 540 GTAACCCCCC TCCCAGAGTT GTGATAACCA AAATGTCTGT AAACATTGCC AAATGTCCCC 600 TGGGGGACAA AATCACCCTG TTGAGAACCA CCACCCTGAA GCCATTCAGC TCCTCAAGAG 660 AAGCATTCTA ACTCCTAGTT CTAGTTATTG AACGCTACAT AACAAACCAC CTCAAAACTT 720 AGTAGCATAA AACAACAACC ATTTTTTGGG CCACTGTCAA GGAGTCAGAA GGGCAATTCT 780 CTGCTCTACG ACGGCTAGGA TGACTGGAAT GACTCGAGGT GACTGGAATA ACTGGGAGTT 840 GGAACAGCTG GGGCTGAAGG GTCCACTTGT AAGATCGTTG TTCACTTGGC AAAGAGAGCT 900 GGAAGGCTGG GCTCAGCTGG GACTGTTGAC CAGAGAGACT ACACATGATG TCTCCAGCAC 960 CATGGCCTGG TCATTGGACC TCTTACGAGG CACCTCAAGT CTCTGGTGTG AGTGTTCTGG 1020 CCAGCAAGAC AGAAGCTGCA TGGCTGTGTA TGTCCCAGCC TTGGAAGTCA CATAGCTCAT 1080 TTCCACTGTA GTCAGAAATC CACACAGGTT CAAGGAAGGA GACACAGACC CACCTCTCCA 1140 TTGGAGAAAT GTCAAAGAAT TTGCAACCAT CTTTTAAATT CACCATACCC TCATCCAGAG 1200 TGATATATAC CTGGGGTGGG GCAGGGCAAG GTAAGTGGGT GGGACATTGA GTCCCACGCT 1260 TCATTCTTCA GACTTTTCCC TCACCTCCCT GTTTTCATCC CTGTATTCAT CTGCCCTCCC 1320 TCCTGCCTGT CTCTCTCCTG TTCAGTGTCT TTGTCTCCAG CTGTGTGGGG CAGGGTGTGG 1380 AGGTGAGACC TGGGGAGGAT TTCAACCAGT TTCCTCCATT CATTACCCCC ACAGGCTGCT 1440 GTACCTCAGC CCCACCAGCC ACAACACCTG GACTCCCCAA GTCTGAGCTC CTCCTGCAGG 1500 GTTCCAGGGG TAAAGTGGCT TGCCTCCTGT CAGTGTGCCC CTCTGCAAGC CCTTCAGAGC 1560 CTAGCTTCCT CCATGTCAGT CATTATTCCT CCACCTGCCT CCCAGCTTCC TGTAGTTTGG 1620 GGAACTCTTT CAGCCACTCA TGTCTCCTTT ACCATTCTCT TTGCCTTTGA GAGTTAATAC 1680 CATTTGGTTG GTTGGTTGTT TGAGACAGAG TCTCGCCTTG TCACCCAAGC TGGAGTGCAG 1740 TGGCACAATC TTGGCTCATT GCAACCTCTG CCTCCTGGGT TCAAGCAATT CTCATATCTC 1800 AGCCTCCCGA GTACCTGGGA CTACAGGCAT GTGCCACCAT GCCTGACTAC TTTTCGTATT 1860 TTTAGTAGAG TCGGGGTTTC ACCATGTTGG CCAAGCTGGT CTCGAACTTC TGATCTCAAG 1920
|