Tag | Content |
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EnhancerAtlas ID | HS143-01668 |
Organism | Homo sapiens |
Tissue/cell | NGP |
Coordinate | chr2:42358920-42361720 |
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 | ZNF263 | MA0528.1 | chr2:42359059-42359080 | GAAGGAGGAATGGAGGAAAAA | + | 6.51 |
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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 | GAGCCAGGAC TCAAACACAG GTTTGCCTGA CAGCCAGACC CTAACCACCC TGCCATTCTG 60 CTGTAGAATG CTTTTCCAGT TAGAAGCCTA TCCAGGGTGG CACCTTCCAT CTCTGTTTCC 120 ATTTTAAAGT GAAAATGCTG AAGGAGGAAT GGAGGAAAAA AAGACAGGTT CATGACCAAA 180 ATTTGACCAC TGTGAGAATT ATGGATAGAT AAGTAGAAAC CTGAAAAGCC ATGAACGACA 240 ACAACAAACT TTAAAAATCA CATCGAATTG AGCAATGGTA AATGCAGAAA TTTGGGATTT 300 ATGGTCGAAA CTGGTGTAGG GACTGGTGGC AACATTTATT TGCAAAGCGT CAAGGACTGC 360 CACCTCCATT TAGATGCCTT TACTACATGA AAGTCTAAAA TACTCTAAAG AGAATCCCGG 420 GAGAGGCTAC AAGCCAAGAA TCTTTGGCTT ACAAAATAGT GGGGGCTGCT TCTTCCCAAG 480 TTACCACGCA CAGAAGCAAA ACTTGGCAGT ATCTGAAACA GAGGATTTTG ATCCTGTTCC 540 TACCATTGCT TCCAGAGAAG GAAGCAAAAC AAACCACTGA GTTCTATCTA CTCCGGCTCC 600 TGAGCACCAA GACCCTGCTT GGAAGAGAAT CTCACCTTGC CGTCTGCTCA GGAAAATCAG 660 CCCCTCTAGA GGAAGCACCA AAAGACCTAA GTGCAGGGCT GGAGTTTCCT ACCCCTTCTT 720 ATTTCCTGTG GAGTTCTGTT TCTTGAGGAA ACTTTCCCCA AATAATCTAG CTGCCACTCT 780 GACACCATTT TCATTGAGTA ATTCATGGTG ATGTCACGCC AACTAGGCAC TAGGGGAAGC 840 CCTGCTTTTA TGGGTTGGCT CTTCATTTAG GAATTTTTAT TTTTCTGACT TCCATCCCTT 900 TTTCACTGGA CTCCACTTTT TTTGAGGCAA GATGCCTGAG TGGTGAAGTG TTGCTTGCTT 960 TTGAGAAAAG GAATTCCTTC TGGTTGAGAG GCAAATGGTT GAGTGAAGGC AAGATGCATG 1020 TCCTGTAATA GTACATCTTA ATTGGAGAGC TGGCAAGAGA GGAAGGAGGT GTGGGCCTGC 1080 TGCGGGCTCT GTTATTCCTA ATAGGGTTCA TTGAGCTAAG CACGGAAGAT GGGCTGGGGG 1140 CACTAGGACT AACAGCCACC CCCTGAAGAC ACAATCACGC ATGCCTGGGG AGCTGACCAC 1200 CTCCTTTTGA CACCTGGACA GCCACATCTA ACCCACATCC CCACGTTCCC GCCTTGCCTC 1260 TCAGCTGCTC TGTGCAGCAA GACAGCAAAG GCAAGTTTGG CAAAGCTCGC CTGTAAAAGC 1320 CTAATCCAAA CAGCATGTCC GCTGAGCTCA GCGGGGTGAC TCATGTGCAG TGATGTGTGA 1380 GGCCAGCGAG CAGAGATTAG GATCTGGCCC GCCCGCCAGC CTACCTTGCA CTTCCTTTGA 1440 TCAACTCTGA TGGTTTTTAA TTCTGCAGAA GCAGCTTCCT GCCAGCAGCA AGCAGCTCTC 1500 AGTGGCGGCT GGAGCTGCGT CTGTGCTGAC CTACTTGTCA GTGGGGAGGG AGGCATGTGC 1560 TAATGGCACT GGGACATCCC GGGCTCACAG GCTACACGGA GCGAGAGGGC AGCCTCTTTT 1620 GCTGAGGTGC CCATGGTGAC ATCAGAAGCT TGCTCCTCAG CCAACACCAG CAAGGCCATG 1680 CGTGTGAGCA GCCTGGGCTC TGAACGTGCT GCTGGTATTG GTTAGAATCA CGGGGTAATC 1740 AAGAAAAATG GGACTCTCCC TGGGGGACTC TTTTTGGGAA ACTGGGGCAT CTCTAAGGAC 1800 GCCATCTGGC ACAAAATGAA GCACTCTCTG GGTTCTTCAG AAGTACTCTT TTACATCTGT 1860 TTTGCTTGAA ATGGAACACA TTCGGAGTAT ATTACTTTTT TGAACCGCTC CTTCCCTGCT 1920 TGGTTGGAAT GCGTTTGCCT CTTGATTCTT CCAAATCCCC TCGATTACCA CTGCCAAGCA 1980 GAGCACCTGA AATCTGGTCT CCTGCTTTCT CATTCCCTCT CTTCCACGTC TCTCCTTTCT 2040 CTCTCTTTTC TCAGGAAGGA TAGCAGTGAT TCTAATCTTG GCTGCATGTT AGCACCACCC 2100 TGGGAAGGGG CTGTGGTTAA AAAAAATTCC CCAGTCCCAG GCTCTGCCCC AGATTAATTC 2160 AGAGTCCTGA GGGTAGGACC AGGCATTAGT ACTGCTTAAA GCTCCTATTG TGGCCAGGCG 2220 CGGTGGCTCA TGCCTGTAAT CCTAGCACTT TGGGAGGCTG TGGCGGGCGG ATTGCCTGAT 2280 CTCAGGAGTT CGTGACCAGC CTGGGCAACA CCGTGAAACC CCATCTCTAC TAAAATGCAA 2340 AAAAATAGCC GGGCATGGCA GCACGCGCCT GTAGTCCCAG CTACTTGGGA GGCTGAGCCA 2400 GGAGAATCGC TTGAACCTGG GAGGCAGAAG TTGCAGTGAG CTGAGATTGC GCCATTGCAC 2460 TCCAGCCTAG GCGACAGAGC GAGACTCCGT CTCCGAAAAA AAAAAAGAAA AGAAACGAAA 2520 AGAAAAAAGA AAAGCTCCCA TTGTGCAGCC AAAGTTAGAA GTCATTGGGA TCTTGGGGTT 2580 GTAGGCCATC AGCCAAAAGC CCTAACAATG GTTCTTATCT GTCCTCCCAC CACCATTCAG 2640 AAGGGTCTAA GAAGTGATGT GTACTTTAAC CACTTAAGGC AAAATATTAT CTGGATGGGA 2700 TAACTAGCCT ACATATTAAG AAGAATTTCT TATTCCGATT AAAAGTATTT ACCGGCTAGG 2760 TGCAGTGGCT CATGCCTATA ATCCCAGAAC TTTGGGAGGC 2800
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