Tag | Content |
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EnhancerAtlas ID | HS197-12896 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr20:17835750-17838080 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr20:17836635-17836653 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr20:17836639-17836657 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr20:17836643-17836661 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr20:17836647-17836665 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr20:17836651-17836669 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr20:17836655-17836673 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr20:17836659-17836677 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr20:17836663-17836681 | GGAGGGAGGGAGGGAGGG | + | 6.03 | Foxq1 | MA0040.1 | chr20:17837861-17837872 | TATTGTTTATT | + | 6.62 | NFAT5 | MA0606.1 | chr20:17836254-17836264 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr20:17836254-17836264 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr20:17836254-17836264 | AATGGAAAAT | - | 6.02 | ZNF263 | MA0528.1 | chr20:17836632-17836653 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 | ZNF263 | MA0528.1 | chr20:17836636-17836657 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 | ZNF263 | MA0528.1 | chr20:17836640-17836661 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 | ZNF263 | MA0528.1 | chr20:17836644-17836665 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 | ZNF263 | MA0528.1 | chr20:17836648-17836669 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 | ZNF263 | MA0528.1 | chr20:17836652-17836673 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 | ZNF263 | MA0528.1 | chr20:17836656-17836677 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 | ZNF263 | MA0528.1 | chr20:17836660-17836681 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_23578 | chr20:17836541-17837830 | Colon_Crypt_1 | SE_24205 | chr20:17836140-17836605 | Colon_Crypt_2 | SE_24205 | chr20:17836657-17838296 | Colon_Crypt_2 | SE_28415 | chr20:17836575-17838324 | Fetal_Intestine | SE_29297 | chr20:17835769-17838534 | Fetal_Intestine_Large | SE_43833 | chr20:17834483-17840297 | MM1S | SE_50301 | chr20:17836651-17837333 | Sigmoid_Colon | SE_50301 | chr20:17837356-17838317 | Sigmoid_Colon | SE_52789 | chr20:17836143-17836626 | Small_Intestine | SE_52789 | chr20:17836668-17837299 | Small_Intestine | SE_52789 | chr20:17837347-17838332 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I017855 | chr20 | 17835904 | 17838967 |
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Enhancer Sequence | CGCCACCATG CCCGGCTAAT TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCATGTTAG 60 CCAGGATGGT CTCGATCTCC TGACCTCGTG ATCCACCTGC CTTGGCCTCC CAAAGTGCTG 120 GGATTACAGG TGTGAGCCAC CATGCCTGGC CTCATGTAAT CCTTTTGATA ACCCTTTGAG 180 ATAAGCACCA AGGGTGTTCC ATAAAACCTA AAAAAAATTA TAGCCAAAAA AAAAAGATTG 240 TTCCAGTACA CATATAACTG AACAAAAAAG TCCTGAAACT GAAAAATGAA AAATCCCAGA 300 AGGTCTGAGT GTAGTGTGGC TGCTTGAGGC CAAATTAGAC CTTCTGGTCA ACATGATTTC 360 CTGTAAGTGA ATAGATAAAA ATAAGCTTCT GTATATGTTC TATGTATTGA ATCATACAGT 420 ATCACTATAT ATGTTTTTTC ATTCAATATT TCTTACAATC CAGCATTGTA AAAGTTTCAC 480 ATGACATGAC ACTTTAGAGG AAGAAATGGA AAATCAGGCT GGATGTGGTG CCTCACACTT 540 GTAATCCCAG CAATTTGGGA GGCCAAGGCC AGAGGATCTG TTGAGCCCAG GAGTTCAAGA 600 CCAGCCTGGG CAACATGGTG AAACCCCATT TCTACAAATA ATAAAAAAAA ATTATCCAAG 660 CATGGTGGTG CATGCCTGTA GTCCCAACTA CTCCAGAGGC TGAGGTGGGA GGGTCACTTG 720 AGCCCAGGAA GTTGAGGATG TAATGAGCCG AGATCATGCC ACTGCACTCC AGCCTGGGTG 780 ACAGAGTGAG ACCCTGTTGA AAGAAAGAGA GAAAGAGAGA AAAGAAAGAA AGAAAAGAAA 840 AAGAGAGAAA GAAAGAAAGA AAGAGAGAGA GAGGGAGACA GAGAGGGAGG GAGGGAGGGA 900 GGGAGGGAGG GAGGGAGGGA GGGAGGGAGG GACAGAAAGA AATGGAAGAT CAGAGAAGTG 960 GAATAACCTC CTAGGATCAC ACAGCTTGTG AATGAGAGGC ACTGAGTTGC TCAGTGATGG 1020 AGTGTCTAAT GTTGGGTGTG TATGTACTGA CTGTGTCCCA AGGCCAATTA TAACTTGGGG 1080 AAGGCACCAC TACCTCCCTG TCATACAATG GGTACATTGT CTGTCAATGG CACGTGGTTG 1140 TACACACCTC CAGGGGTAAA CAATCAAAAG TCAGGAGCCT CTCCAGCTCT CCCTCATAAA 1200 AATACTGTAT CCTCTAGGGA GTGGGGTTCT CTAGTCCAGC CCCATGTGAT ATGCAGTCCC 1260 AGTGGGGCCG GGAGATTTGC CCAAGGTCAC ACAGCTGGTT AGAGGGGAAC CACACACCAC 1320 CACGTCCTGC AGCTGCAAAT CTGTTTCATG GCCTGCTTCC TCTCTTCTTC CCTAGAATGC 1380 CTTTTTTTTC TACCACAGAG TTTCTACAGT TCAAACCTGG AGGGCAGGTT GGGTTTTGTT 1440 TTGTTTTTCA CACACTCCTT CACAGATTAC AGGAGAGATT TTACTCTTGA ACTGAAAGTA 1500 GAAAATTATT GTTAGCTTTA ACACACAGCT CTTTCTCTCT TCCCCAACCC AGATACATTA 1560 GGATCCTCTT GTCCTATCAA AAAAAAAATA GTAATAATAA TAATAATAAT AATAATAATA 1620 ATTCTATGGG GCAGAAAAGA GAAGAATTTG TGAGTTTCCC ATTCCTGGCT GGACATTTCC 1680 CACAAATGGC AGTTAAGTCT TCATTGACTA ATAGGAAAAG AGCAGCTCCA GCCGCATGAC 1740 TTCACGGCAC AGGCAAAGTC AAAGGCAAGG AGAGCTCACC TTAACTCTGG TGTATAGACA 1800 CAGACTCCAT GCCTCTTGTC CAACTCTTCC ATCAGGGAGC CAGAACGTCC ACATCTTCCA 1860 GGTTCCTGTA GGCTGTGTTT AGGGAGAGAT GTAAGACTCT ACTGGAACTT ACGTGCTGGG 1920 AGGGCCAATG GTGCTGACAC TTGGTCTTCT TGCTCTTGGC TGATGGATAG CAGGGAATAT 1980 GAAGCTATCT ATATCTCACT CAGATAGAGA TGGACATTCC AGTCAAAAGC TAAGCTACTT 2040 CTGAATGCAA AGATGGTGTA TCAGCTTTTG CTGCATAACA AACCACTCCA AAATGTAGTG 2100 GTTAAAATAA CTATTGTTTA TTTAGCTCAT GAGTCCTCAT ATTAGCCATT TGGGTTGTGC 2160 TTAGCTGGGC TCATTCCTAT GTCTTTGGTC AGCTGCTGGG TTTGCTGGGC CTGTCTGATC 2220 TGGGATGGCT CAGCTGAGAC AGTATGCCTC TGCTCCACGT GGTCTCTCAT CCTCAGCAGC 2280 ATAGCCTGAG CTTTATGCAC AGTAGCCTGG GCTTTATCCA TGGTAACCAA 2330
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