Tag | Content |
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EnhancerAtlas ID | HS060-03329 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr10:3802960-3804440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr10:3803746-3803757 | AAGCAATAAAA | + | 6.32 | EWSR1-FLI1 | MA0149.1 | chr10:3803012-3803030 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr10:3803016-3803034 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr10:3803036-3803054 | CCCTCCTTCCTTCCCTCT | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr10:3803060-3803078 | CCTTCCTTCCTTCTTCTC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr10:3803052-3803070 | CTCTACTTCCTTCCTTCC | - | 7.39 | EWSR1-FLI1 | MA0149.1 | chr10:3803032-3803050 | CCCTCCCTCCTTCCTTCC | - | 7.97 | EWSR1-FLI1 | MA0149.1 | chr10:3803056-3803074 | ACTTCCTTCCTTCCTTCT | - | 8.08 | EWSR1-FLI1 | MA0149.1 | chr10:3803028-3803046 | CCTTCCCTCCCTCCTTCC | - | 8.15 | EWSR1-FLI1 | MA0149.1 | chr10:3803024-3803042 | CCTTCCTTCCCTCCCTCC | - | 8.45 | EWSR1-FLI1 | MA0149.1 | chr10:3803008-3803026 | ATTTCCTTCCTTCCTTCC | - | 9.03 | EWSR1-FLI1 | MA0149.1 | chr10:3803020-3803038 | CCTTCCTTCCTTCCCTCC | - | 9.47 | Foxd3 | MA0041.1 | chr10:3803669-3803681 | GAATGTTTTTTT | + | 6.52 | Gabpa | MA0062.2 | chr10:3803818-3803829 | CCCACTTCCGG | - | 6.02 | NFYB | MA0502.1 | chr10:3803472-3803487 | ACCCCAGCCAATCAG | + | 6.3 | ZBTB7A | MA0750.2 | chr10:3803818-3803831 | CCCACTTCCGGGG | - | 6.92 | ZNF263 | MA0528.1 | chr10:3803044-3803065 | CCTTCCCTCTCTACTTCCTTC | - | 6.16 | ZNF263 | MA0528.1 | chr10:3803016-3803037 | CCTTCCTTCCTTCCTTCCCTC | - | 6.24 | ZNF263 | MA0528.1 | chr10:3803032-3803053 | CCCTCCCTCCTTCCTTCCCTC | - | 6.25 | ZNF263 | MA0528.1 | chr10:3803012-3803033 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr10:3803020-3803041 | CCTTCCTTCCTTCCCTCCCTC | - | 7.27 | ZNF263 | MA0528.1 | chr10:3803028-3803049 | CCTTCCCTCCCTCCTTCCTTC | - | 7.28 | ZNF263 | MA0528.1 | chr10:3803024-3803045 | CCTTCCTTCCCTCCCTCCTTC | - | 8.92 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09469 | chr10:3801193-3805066 | CD14 | SE_11200 | chr10:3798685-3804931 | CD20 | SE_18262 | chr10:3802549-3805299 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19173 | chr10:3802652-3805366 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20046 | chr10:3802640-3804587 | CD56 | SE_26609 | chr10:3803129-3807958 | Esophagus | SE_35818 | chr10:3803696-3807111 | HMEC | SE_47115 | chr10:3803313-3809407 | Panc1 | SE_53372 | chr10:3802899-3803998 | Spleen | SE_62321 | chr10:3783568-3829344 | Tonsil | SE_64224 | chr10:3803544-3807611 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I003760 | chr10 | 3802724 | 3809069 |
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Enhancer Sequence | GGCTAATTGT GGCCAGCGTT TTATTCTTCA AGGTGCAGAA AAACATACAT TTCCTTCCTT 60 CCTTCCTTCC TTCCCTCCCT CCTTCCTTCC CTCTCTACTT CCTTCCTTCC TTCTTCTCTC 120 TTTCTCTCTC TTTCTTGCTT TCTTTAGCCT GTGCAGGAGT CAGACTCTGT ATTGCATTTA 180 GAATGAAGAT AAGTCAAATT TTTAATCCCT GAGCCAAACA CATCGGGTAA CTTTCAAGTT 240 CCCCAGAATC TTCTGATTTT CACTTGGGTT CAAAACCACA GTTCCACATG CAGTTGAAGT 300 GGCATTTTCT TCCATTGGCA ACTTCTGCAT TTGGTATCAA ACCTTTGGTT ATGCACAGAG 360 CTGAGGGAGA GCAAACCGAT TCTTCACGCA TGTTCCACCC TTGGAGCACT CACCCCTACC 420 TCTAGGAGAG CCCCTAAAAT GAGCTTGAGT CCTCCATCCA GAAACGAACC AACACTTCTC 480 ACAGAGAAGA TGGCAGGGCC TCGTGCATCA GAACCCCAGC CAATCAGGAC TGCAAATAAA 540 TACCCAGAAG CTGGTCTCAA TGATGCGCTT GGTATAGGAA ATGAAAGACG GAACCAATGG 600 TTTCAACAAA ATGAGAGCAG AACTGAAAGT CTGCAAATAA AAATTACAGG TCCTTCATCA 660 CAGCTTTCCC TCCACACAGG CCGTAAGAAA ACCATGCAGT TCTCTAAGAG AATGTTTTTT 720 TTTTTTTTTT TCCAAGAGCT CTTGAGTCAT CTTGGTTTCT GTCTCTTGAT GTAGAATTGA 780 CTCTGAAAGC AATAAAATAG TAAAAACACC TCATTCCCCT GCTTTGCATG TAATGGACTA 840 ACCAGGAAGA TAAAATGTCC CACTTCCGGG GCTCTTCACC TGACATCACC TTAGTTTGAA 900 GTTACTTAGC TTGGTATTCT GGCATATTTT AGAAAGCAAA AAGCACCTTA AACCTTAACA 960 TTTTGTGTCA TTTCTAGGCC AAACACTTTG GGGCTTTTAA AAAAAGTACA CCAAGATAAA 1020 GTCATCATTG ACTCTGTTGA AAGAAATGGT AGGCAAAAAT AAATAAATAA ATAAATTTGA 1080 CAAATGTATT AAAAATTCAA GGCTAAATGG GTTGAACAAA AGATTGGAAG CCGAGGTAAT 1140 CTGTGAGAGA TCCATGCCCA GCTGGCTAAG CTTTTCATCC TTCGGTTCTT ACCCCTGACT 1200 TGCTGAACCA GCATGGTTAG AAAATGTGGG CCACACACAC AAACAACGTT GAAATTCCTT 1260 GGATGTCAAG CTTTTGATTC ACGCCCATTC TGTAAAGCAT TAGGAGGTCA AAGGTGTATG 1320 GTTTTCTGCA CTTTGGAAAA GAAGGAGCTG ACCATTTCCA GCCTTCAGTG CTCTCTTTCA 1380 TGCTAATAAT TGAGCTGGAA TTCCTGAAGA ATGACACTGG GCGCTGAGGT TCGTCCTGGG 1440 AAGTAGGGGT GGGGTTTGTA CCTGCAGTTT GCATAGGATC 1480
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