Tag | Content |
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EnhancerAtlas ID | HS020-30776 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr3:45166200-45168840 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:45166629-45166647 | GGAAGGACAGATGGAAGG | + | 6.49 | EWSR1-FLI1 | MA0149.1 | chr3:45167685-45167703 | CTTTCTTTCTTTCCTTCC | - | 6.95 | EWSR1-FLI1 | MA0149.1 | chr3:45167729-45167747 | CCTTCCTTCCTTCTTCTC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr3:45167709-45167727 | CTTTCTTTCCTTCCTTTC | - | 7.36 | EWSR1-FLI1 | MA0149.1 | chr3:45167705-45167723 | CCTTCTTTCTTTCCTTCC | - | 7.69 | EWSR1-FLI1 | MA0149.1 | chr3:45167697-45167715 | CCTTCCTTCCTTCTTTCT | - | 7.85 | EWSR1-FLI1 | MA0149.1 | chr3:45167701-45167719 | CCTTCCTTCTTTCTTTCC | - | 7.87 | EWSR1-FLI1 | MA0149.1 | chr3:45167725-45167743 | TCTTCCTTCCTTCCTTCT | - | 8.2 | EWSR1-FLI1 | MA0149.1 | chr3:45167689-45167707 | CTTTCTTTCCTTCCTTCC | - | 8.46 | EWSR1-FLI1 | MA0149.1 | chr3:45167693-45167711 | CTTTCCTTCCTTCCTTCT | - | 8.46 | EWSR1-FLI1 | MA0149.1 | chr3:45167713-45167731 | CTTTCCTTCCTTTCTTCC | - | 8.99 | EWSR1-FLI1 | MA0149.1 | chr3:45167717-45167735 | CCTTCCTTTCTTCCTTCC | - | 9.25 | EWSR1-FLI1 | MA0149.1 | chr3:45167721-45167739 | CCTTTCTTCCTTCCTTCC | - | 9.25 | ZNF263 | MA0528.1 | chr3:45167685-45167706 | CTTTCTTTCTTTCCTTCCTTC | - | 6.02 | ZNF263 | MA0528.1 | chr3:45167689-45167710 | CTTTCTTTCCTTCCTTCCTTC | - | 6.03 | ZNF263 | MA0528.1 | chr3:45167724-45167745 | TTCTTCCTTCCTTCCTTCTTC | - | 6.05 | ZNF263 | MA0528.1 | chr3:45167721-45167742 | CCTTTCTTCCTTCCTTCCTTC | - | 6.28 | ZNF263 | MA0528.1 | chr3:45167717-45167738 | CCTTCCTTTCTTCCTTCCTTC | - | 6.54 | ZNF263 | MA0528.1 | chr3:45167713-45167734 | CTTTCCTTCCTTTCTTCCTTC | - | 6.68 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_23409 | chr3:45164183-45167627 | Colon_Crypt_1 | SE_23409 | chr3:45167735-45168211 | Colon_Crypt_1 | SE_24554 | chr3:45166631-45166987 | Colon_Crypt_2 | SE_24554 | chr3:45167076-45167617 | Colon_Crypt_2 | SE_24554 | chr3:45167775-45168120 | Colon_Crypt_2 | SE_26951 | chr3:45163928-45170032 | Esophagus | SE_34427 | chr3:45163922-45170188 | HCT-116 | SE_34949 | chr3:45163595-45169924 | HeLa | SE_35922 | chr3:45163785-45169894 | HMEC | SE_39339 | chr3:45163841-45167620 | IMR90 | SE_39859 | chr3:45166940-45168353 | K562 | SE_44835 | chr3:45164022-45168245 | NHLF | SE_46103 | chr3:45163942-45168295 | Osteoblasts | SE_50396 | chr3:45164648-45167634 | Sigmoid_Colon | SE_50396 | chr3:45167738-45168277 | Sigmoid_Colon | SE_52910 | chr3:45163843-45168625 | Small_Intestine | SE_55649 | chr3:45159167-45170173 | u87 | SE_64277 | chr3:45163939-45170076 | NHEK | SE_67446 | chr3:45159167-45170173 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I045117 | chr3 | 45159147 | 45169814 |
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Enhancer Sequence | CTGAGCATCA GATAAGTCGT GATATGCTTT TAGGGGCCAG GTTTGCAAAA TACGTTTCAT 60 TAAATTGTGG ATGTGCACAC CATGGGAGCC CCAGGATGTC CAGCAGATTG GCAAGTTTAT 120 ACCCTACCTC ATATCCACCC CAAGGGGACA CACACACCAT TGCAATGATT TCTCCCAACC 180 TTTATTCCCT GCAGGGAGCG AGTGTTGAAT TCACACACAT TGAATGAACA TTTGCCTGTC 240 TGTTCATTAG ACCCAAATAG TAATTTTAGG ACACCAGGGA ACTTCAAGGT ACTCTGAAGA 300 CATTGAGGGT CTGCTATCAA CCATCTGGGG GTGGTGGTCA AGGAGGGCTT CACAGAAGGC 360 GTATGACTTA AGATGGGTCT AAAAGAATGG ATATGAGTGT GCCAACCAGG AACTGTGAGA 420 TGACTGTCAG GAAGGACAGA TGGAAGGAAT AGCAGGTGCA AAGATGCCAA GATATGAAAA 480 TCATGGCTTC CTTGGAGCCA CTCTGGGGAG TTTGATTTGG CCAGAGTTTT GTTTGGGTGG 540 GTAGAGGAGG CTGGAGAAGT GGGAAAGGGC TTGGTTGTTG GCCACGGAGT TTGGGCTTCA 600 CCCACTGGGA CCAGCACACC TTAGCAGCTT GGTGTGGTGG TGAAGAGTAC AGATTCTAGA 660 ATCAAACTGT CTAGGGTCAA TTCCCGGCAC TACCACTCAC CCAGATGTGC TTCCTTGGGC 720 AAATTCCTTA GCTTCTTGGT GCCTCACTTT CCTCATCTGC AAACAGGATA ATAATGAAAT 780 TCCTGTAAGG CCTAAATGAG TTAATACCTA CAAAGTGCTT AGAATGGTGC CAGGTAGTCA 840 ATCAATATTG GCTGTTAGTA TTGTTGATAT TATCAATGAT AGCATATTAC AACTACTACT 900 AGCAGCGATG GGGCACCATT GAAGGGTGCT AAGCAGACAA CTATAGCAGC AGTTTGGCTC 960 TGAGTCTAAA GCCTACAGTC CTGGCTGGCT GGGTGGGGAC TACGTAAGGC AGGCAAAGCA 1020 CTGAAGAGGC AAACCTTAAG GAGGCACTCA CTGTCAGGGC AGTGCCACTT AAGGAAGCAA 1080 GTATGAGTGC CTCCTTAAAT TCTGCACACC TTATCTGCCT CACCTAGCCA TGGCCCTGGC 1140 CCTGATCATT GGCTATTAAT AGGCCCTTCT ACATGTTGAC TCATGTGACT CCAGCACCCT 1200 CACTGAGACC AGAGAAGTGA CCTCCCTTCT CCAAGTTTGC TGAACTCAGG AGGCAGCTGG 1260 GACATTCTGG TTCAACCCTG GCACCTCTGC AGTCTCCACC CACCCAGGGT ACCACAATGA 1320 GCTGCCCTCA TAGAAGCTGC CAAGGCTGGT CAAGTTACCT AGCAGAAGAG GAGCAACTGC 1380 TGCCATTCTT TGTCTCTCTC TCTTTCTTTC TTTCTTTCTT TCTTTCTTTC TTTCTTTCTT 1440 TCTTTCTTTC TTTCTTTCTT TCTTTCCTTC TTTCTCTCTC TCTCTCTTTC TTTCTTTCCT 1500 TCCTTCCTTC TTTCTTTCCT TCCTTTCTTC CTTCCTTCCT TCTTCTCTCT CTCTCTCTCT 1560 GTTTCTTTTT TTTGTCTACC CTGGAGGTGA CAGAAACTGC CATTCTTATT AAGTGAATGC 1620 AGTTGTTGGC TGATTCCAGG AAGTGGGGAG TCACCTCCAA CAGAATTCAT TCTAACAGTG 1680 CCTGCTGTGG GAGGGGTGGG GGTGCCAGAT AGTCACATCG CCAAACTTGG AGTCTTCCTA 1740 GTCCAGTGGA CCTGAGGCAG TGAGGCCTAA AGGCATAGAG AGACAACTGG TTTAGACACT 1800 CAAAATCCAC GTGTCATTGA CTTGGCCGGG TCCATTTACA GACTGGTAAA TTGAGGTGTA 1860 AGTCTTGCCA ACAACAGGAA GACCACTGAT CTGCCTACCT GGAAATAGTT CATTTCCACC 1920 TTCACATAAG AAAGAACTAG AACATGAATT GCCATTTCAA GGGCTAATCA TTCTCTCTTG 1980 GATGGGAGAA AAACCTTTGG AATCTAGACA CCAGGCCTGT CTAAATAGTA ACAACAACAA 2040 ACATTTAATG ATTCCTTAAT ATTAGGCAGC CCCGTGCATA TGTTTATAAA TATTTATAAA 2100 TCCCCACAAC CACTCCATAA AGTAGGTTCT AATATTAAAC CCCATTGTAC AGATGAAGAA 2160 ACTGAGGCTT GGGTAGGTTA AGTAATGTAC CCAGGCATAT ATGATTAATA AGAGGTAGAG 2220 ACAAGTTTTG TGTCCCAGCT CTGACACCGG TGCCCGGGGC ATGATAAATG ACTATTCATC 2280 AGAGCTAGCC CCGCCCGAAG AACTCCACAC ACAACCAGGA ACTTTCTGAT GATGGTGCGT 2340 TGTTCTTACC AACAAAGTCA ATCAAGGTAG AATGAAGTAT TTCCAAGCTG CTGGCTTTCT 2400 AGGATATCAA AAGGAAAACA TATTTGTTTT AAATGGTCCA ACAAGCACAC TGTATTACTG 2460 CAAATCCTCC TTCATGTCAA AGTAATTTGA AAGTATAGTT GGAATTTAAG CTTAAGATTT 2520 AAATTCCACA GAATTTGAAA TGTTTGGGGC GTGGTTGTTC TTTTGTATTG TTCTTTTTTG 2580 GCAGTGCCAG GTGTAAGGTT CTAAGAAAGG GAACTGGCAT GGTTCCACTG CTGATGGCTC 2640
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