Tag | Content |
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EnhancerAtlas ID | HS108-22044 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:42359100-42361870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr2:42360274-42360285 | GGTGACTCATG | + | 6.62 | FOSL2 | MA0478.1 | chr2:42360273-42360284 | GGGTGACTCAT | + | 6.14 | GATA2 | MA0036.3 | chr2:42361531-42361542 | TTCTTATCTGT | + | 6.14 | Gata1 | MA0035.3 | chr2:42361531-42361542 | TTCTTATCTGT | + | 6.62 | JUNB | MA0490.1 | chr2:42360273-42360284 | GGGTGACTCAT | + | 6.32 | JUND | MA0491.1 | chr2:42360274-42360285 | GGTGACTCATG | + | 6.02 | Nkx3-2 | MA0122.3 | chr2:42361585-42361598 | TTAACCACTTAAG | + | 6.5 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_00451 | chr2:42357045-42361304 | Adipose_Nuclei | SE_10312 | chr2:42359605-42361300 | CD19_Primary | SE_11146 | chr2:42359293-42361651 | CD20 | SE_12114 | chr2:42358231-42361528 | CD3 | SE_14693 | chr2:42358043-42361495 | CD4_Memory_Primary_7pool | SE_17117 | chr2:42358116-42361835 | CD4p_CD225int_CD127p_Tmem | SE_17444 | chr2:42358157-42362083 | CD4p_CD25-_CD45RAp_Naive | SE_17811 | chr2:42350038-42364463 | CD4p_CD25-_CD45ROp_Memory | SE_18685 | chr2:42352740-42361648 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20190 | chr2:42358499-42361531 | CD56 | SE_22420 | chr2:42357917-42361491 | CD8_primiary | SE_30543 | chr2:42359109-42360971 | Fetal_Muscle | SE_34033 | chr2:42359215-42361165 | HCC1954 | SE_46062 | chr2:42358081-42361499 | Osteoblasts | SE_47323 | chr2:42352165-42361721 | Panc1 | SE_50137 | chr2:42358847-42361245 | Sigmoid_Colon | SE_53105 | chr2:42358726-42361240 | Small_Intestine | SE_53609 | chr2:42358880-42361233 | Spleen | SE_62313 | chr2:42323195-42370065 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr2 | 42359305 | 42361097 | chr2 | 42359577 | 42359846 | chr2 | 42360195 | 42360705 | chr2 | 42361000 | 42361265 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I042123 | chr2 | 42350301 | 42367048 |
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Enhancer Sequence | ATTTGACCAC TGTGAGAATT ATGGATAGAT AAGTAGAAAC CTGAAAAGCC ATGAACGACA 60 ACAACAAACT TTAAAAATCA CATCGAATTG AGCAATGGTA AATGCAGAAA TTTGGGATTT 120 ATGGTCGAAA CTGGTGTAGG GACTGGTGGC AACATTTATT TGCAAAGCGT CAAGGACTGC 180 CACCTCCATT TAGATGCCTT TACTACATGA AAGTCTAAAA TACTCTAAAG AGAATCCCGG 240 GAGAGGCTAC AAGCCAAGAA TCTTTGGCTT ACAAAATAGT GGGGGCTGCT TCTTCCCAAG 300 TTACCACGCA CAGAAGCAAA ACTTGGCAGT ATCTGAAACA GAGGATTTTG ATCCTGTTCC 360 TACCATTGCT TCCAGAGAAG GAAGCAAAAC AAACCACTGA GTTCTATCTA CTCCGGCTCC 420 TGAGCACCAA GACCCTGCTT GGAAGAGAAT CTCACCTTGC CGTCTGCTCA GGAAAATCAG 480 CCCCTCTAGA GGAAGCACCA AAAGACCTAA GTGCAGGGCT GGAGTTTCCT ACCCCTTCTT 540 ATTTCCTGTG GAGTTCTGTT TCTTGAGGAA ACTTTCCCCA AATAATCTAG CTGCCACTCT 600 GACACCATTT TCATTGAGTA ATTCATGGTG ATGTCACGCC AACTAGGCAC TAGGGGAAGC 660 CCTGCTTTTA TGGGTTGGCT CTTCATTTAG GAATTTTTAT TTTTCTGACT TCCATCCCTT 720 TTTCACTGGA CTCCACTTTT TTTGAGGCAA GATGCCTGAG TGGTGAAGTG TTGCTTGCTT 780 TTGAGAAAAG GAATTCCTTC TGGTTGAGAG GCAAATGGTT GAGTGAAGGC AAGATGCATG 840 TCCTGTAATA GTACATCTTA ATTGGAGAGC TGGCAAGAGA GGAAGGAGGT GTGGGCCTGC 900 TGCGGGCTCT GTTATTCCTA ATAGGGTTCA TTGAGCTAAG CACGGAAGAT GGGCTGGGGG 960 CACTAGGACT AACAGCCACC CCCTGAAGAC ACAATCACGC ATGCCTGGGG AGCTGACCAC 1020 CTCCTTTTGA CACCTGGACA GCCACATCTA ACCCACATCC CCACGTTCCC GCCTTGCCTC 1080 TCAGCTGCTC TGTGCAGCAA GACAGCAAAG GCAAGTTTGG CAAAGCTCGC CTGTAAAAGC 1140 CTAATCCAAA CAGCATGTCC GCTGAGCTCA GCGGGGTGAC TCATGTGCAG TGATGTGTGA 1200 GGCCAGCGAG CAGAGATTAG GATCTGGCCC GCCCGCCAGC CTACCTTGCA CTTCCTTTGA 1260 TCAACTCTGA TGGTTTTTAA TTCTGCAGAA GCAGCTTCCT GCCAGCAGCA AGCAGCTCTC 1320 AGTGGCGGCT GGAGCTGCGT CTGTGCTGAC CTACTTGTCA GTGGGGAGGG AGGCATGTGC 1380 TAATGGCACT GGGACATCCC GGGCTCACAG GCTACACGGA GCGAGAGGGC AGCCTCTTTT 1440 GCTGAGGTGC CCATGGTGAC ATCAGAAGCT TGCTCCTCAG CCAACACCAG CAAGGCCATG 1500 CGTGTGAGCA GCCTGGGCTC TGAACGTGCT GCTGGTATTG GTTAGAATCA CGGGGTAATC 1560 AAGAAAAATG GGACTCTCCC TGGGGGACTC TTTTTGGGAA ACTGGGGCAT CTCTAAGGAC 1620 GCCATCTGGC ACAAAATGAA GCACTCTCTG GGTTCTTCAG AAGTACTCTT TTACATCTGT 1680 TTTGCTTGAA ATGGAACACA TTCGGAGTAT ATTACTTTTT TGAACCGCTC CTTCCCTGCT 1740 TGGTTGGAAT GCGTTTGCCT CTTGATTCTT CCAAATCCCC TCGATTACCA CTGCCAAGCA 1800 GAGCACCTGA AATCTGGTCT CCTGCTTTCT CATTCCCTCT CTTCCACGTC TCTCCTTTCT 1860 CTCTCTTTTC TCAGGAAGGA TAGCAGTGAT TCTAATCTTG GCTGCATGTT AGCACCACCC 1920 TGGGAAGGGG CTGTGGTTAA AAAAAATTCC CCAGTCCCAG GCTCTGCCCC AGATTAATTC 1980 AGAGTCCTGA GGGTAGGACC AGGCATTAGT ACTGCTTAAA GCTCCTATTG TGGCCAGGCG 2040 CGGTGGCTCA TGCCTGTAAT CCTAGCACTT TGGGAGGCTG TGGCGGGCGG ATTGCCTGAT 2100 CTCAGGAGTT CGTGACCAGC CTGGGCAACA CCGTGAAACC CCATCTCTAC TAAAATGCAA 2160 AAAAATAGCC GGGCATGGCA GCACGCGCCT GTAGTCCCAG CTACTTGGGA GGCTGAGCCA 2220 GGAGAATCGC TTGAACCTGG GAGGCAGAAG TTGCAGTGAG CTGAGATTGC GCCATTGCAC 2280 TCCAGCCTAG GCGACAGAGC GAGACTCCGT CTCCGAAAAA AAAAAAGAAA AGAAACGAAA 2340 AGAAAAAAGA AAAGCTCCCA TTGTGCAGCC AAAGTTAGAA GTCATTGGGA TCTTGGGGTT 2400 GTAGGCCATC AGCCAAAAGC CCTAACAATG GTTCTTATCT GTCCTCCCAC CACCATTCAG 2460 AAGGGTCTAA GAAGTGATGT GTACTTTAAC CACTTAAGGC AAAATATTAT CTGGATGGGA 2520 TAACTAGCCT ACATATTAAG AAGAATTTCT TATTCCGATT AAAAGTATTT ACCGGCTAGG 2580 TGCAGTGGCT CATGCCTATA ATCCCAGAAC TTTGGGAGGC CAAGGCAGGA GGACCGCTTG 2640 AGCCTAGGAA TTCAAGACCA GCCTGGGCAA CATAGTGAGA CCCTTGTCTC TACAAAAAAT 2700 AAAATAAAAA ATTAGCCCAA GCATGGTGAC GTGTGCCTGT GGTCTCAGCT ACTCGGGAGG 2760 CTGAGGTGGG 2770
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