Tag | Content |
---|
EnhancerAtlas ID | HS182-09497 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:44260100-44261800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:44260998-44261016 | AGAAGGAAGGAGGGAGGG | + | 6.62 | EWSR1-FLI1 | MA0149.1 | chr17:44261010-44261028 | GGAGGGAAGGAAGGGAAG | + | 7.26 | EWSR1-FLI1 | MA0149.1 | chr17:44260990-44261008 | GGAGGGAAAGAAGGAAGG | + | 7.87 | EWSR1-FLI1 | MA0149.1 | chr17:44261002-44261020 | GGAAGGAGGGAGGGAAGG | + | 8.15 | EWSR1-FLI1 | MA0149.1 | chr17:44260994-44261012 | GGAAAGAAGGAAGGAGGG | + | 8.34 | EWSR1-FLI1 | MA0149.1 | chr17:44261006-44261024 | GGAGGGAGGGAAGGAAGG | + | 8.45 | Nr5a2 | MA0505.1 | chr17:44260579-44260594 | GAGTTCAAGGCCAGC | + | 8.25 | TBX20 | MA0689.1 | chr17:44261511-44261522 | TAGGTGTGAAG | + | 6.62 | ZNF263 | MA0528.1 | chr17:44260948-44260969 | AGAGGAGACAGGGGAGAGGGG | + | 6.12 | ZNF263 | MA0528.1 | chr17:44260934-44260955 | AGAGGAGAGAGGAGAGAGGAG | + | 6.16 | ZNF263 | MA0528.1 | chr17:44261015-44261036 | GAAGGAAGGGAAGGAGTAGGG | + | 6.33 | ZNF263 | MA0528.1 | chr17:44260924-44260945 | AGGGGAGGAGAGAGGAGAGAG | + | 6.36 | ZNF263 | MA0528.1 | chr17:44260917-44260938 | AGAGGAGAGGGGAGGAGAGAG | + | 6.41 | ZNF263 | MA0528.1 | chr17:44261007-44261028 | GAGGGAGGGAAGGAAGGGAAG | + | 6.61 | ZNF263 | MA0528.1 | chr17:44260927-44260948 | GGAGGAGAGAGGAGAGAGGAG | + | 6.94 | ZNF263 | MA0528.1 | chr17:44260987-44261008 | AAAGGAGGGAAAGAAGGAAGG | + | 7.17 | ZNF263 | MA0528.1 | chr17:44260999-44261020 | GAAGGAAGGAGGGAGGGAAGG | + | 7.28 | ZNF263 | MA0528.1 | chr17:44261003-44261024 | GAAGGAGGGAGGGAAGGAAGG | + | 8.92 |
|
| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_09447 | chr17:44258026-44260944 | CD14 | SE_09447 | chr17:44261055-44263259 | CD14 | SE_11745 | chr17:44257972-44261125 | CD20 | SE_18395 | chr17:44261243-44262664 | CD4p_CD25-_Il17-_PMAstim_Th | SE_60799 | chr17:44255747-44273300 | DHL6 | SE_63056 | chr17:44256345-44273776 | Tonsil |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr17 | 44260792 | 44260850 | chr17 | 44261560 | 44261685 | chr17 | 44260375 | 44260555 | chr17 | 44260913 | 44261022 |
|
| Number: 3 | ID | Chromosome | Start | End |
GH17I046182 | chr17 | 44260341 | 44260550 | GH17I046183 | chr17 | 44260667 | 44261204 | GH17I046184 | chr17 | 44261244 | 44262664 |
|
Enhancer Sequence | GATGCTCAAA GAAGTTAAGT AATTTGCCCA TGATCACACA ACTATGAAGT TGCAGGGGCA 60 GGATCCATAA TGCTAAAGCC GATGCTTTTA ACTACTACAC TAGATAGTTT AAGGCTTAAA 120 CTGAAACGGT CTTAACTGCC TGACAGTAAA TTCTGAATTT TAGTCTTTAG AGGAAAGTCA 180 GTCAAAGAAC ACCAACTACC TACTGAGTAT CTCCAATAAA TATTAAAATG CCTAGAGTAT 240 TCAAAGCACC ACAGTAAGTA CATACAAGGA TGACAAGCAG CAGTAAAGAG AGACACTACT 300 GTGTGATTTG GGGGATGGAG GCAATCCTCA TACAGGCTGA GAAGTAGGCG GAGTCAGAAA 360 ATGCTTTTCA GAAAAAAGAA CATCCAGGCT GAAACCTAAA GAATGAGTAG GAGCTGGGTG 420 CAGTGGCAGG CGCCTGTATT TCCAGTTACT CAGGAGGCAG GAGGATGGCT TCAGGCAAGG 480 AGTTCAAGGC CAGCCTAGGC AACATAGCCC CCATCTAAAA AAGCCACCCA AACAAAAACA 540 CTAATTTTTT TTTTTTAAAT GATGGCCTAC CATGGTAGCT CACACTTATA AGCCCAGCAC 600 CTTGGGAGGC CAAGGCAGGA GGATCGCCTG AGCCCAGGAG GAGTTTGAGA CTAGCCTAGA 660 CAACACACTG AGACCCAGTC TCTAAAAAAA TAATAATTAG CTGGGCATAG TGGGAGGGTC 720 ACTTGAGCCT GGCGGGTGGA GGTCGCAGTG AGCTGTTATC ACGCCACTGC ACTCCAGCCT 780 GGGTTACAGA GCAAGATTCT GTCTCAAAAG AAGGAAAAGA GGAGAGGGGA GGAGAGAGGA 840 GAGAGGAGAG AGGAGACAGG GGAGAGGGGA GAGGAGGTGA GAGAAGAAAA GGAGGGAAAG 900 AAGGAAGGAG GGAGGGAAGG AAGGGAAGGA GTAGGGCCGG GAGAGGTGGC TCACGCCTGT 960 AATTCCAGCA CTTTGGGAGG CCAAGGCAGG AAGATCACTT GAGGTCAGGA GTTTGAGACC 1020 AGCCTGGCCA ACACAGCGAA ACCCCGTCTT TGCCTGTAAT CCCAGCTATT CAGAAGGCTG 1080 AGGTACAAGA ATCACCTGAA TCTGGGAGGC AGCGGCTGCA GTGAGCTGAG ATGGCACCAC 1140 TGCACTCCAG CGTAGGCGAC AGAATGAGAC TGTCTCCAAA AAAACAAAAA GAAAGAAATG 1200 AGTAGAATTC AGCATTGCCT ATACAACTAC TTCAAGCATC CCATATTCAA AACCCATTCC 1260 CTGCCCCAAC ACCAAATCCA AAACTTCCTC CTGCTCCTCA ACATTGTCTA TTTGAGTTAA 1320 TCATGACCTC AAATCACCAA CTTACTTTTT ACCATAAATA TTTAATTTAA ACATCTACTA 1380 AATGCCAGAT ACAAGATAGT AAAATATAAA TTAGGTGTGA AGGTAGCCTA GCTTGATAAA 1440 GTACTGTATT TCACCTGAAG GGGTCAAGGA AGGCTTCTAG AAAAGATGAC ATACTGACTG 1500 AATTTTGAAA GGTGAGGTGG TGCACAGAGG GTGAGGGTTG GCAACACACA GAATGACAGG 1560 CACATTCATT CCATCCTTGG TGCCAATGCC CTAGTGCAGA ACCTCATTAT GTACTATAGT 1620 AATTCAGGCA GTAATAATCT CCCAACTATT CTTCCTTCTT CCTGTCTCAG CAAGCCTCTA 1680 ATCTAGCGTC CACTACCAAA 1700
|