Tag | Content |
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EnhancerAtlas ID | HS110-00556 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr11:17007650-17009340 |
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) |
EWSR1-FLI1 | MA0149.1 | chr11:17008409-17008427 | GGAAGGGAGGCAGGAAAG | + | 7.67 | IRF1 | MA0050.2 | chr11:17008138-17008159 | TATTTATTTCACTTTCACTTT | + | 6.96 | PRDM1 | MA0508.2 | chr11:17008146-17008156 | TCACTTTCAC | + | 6.02 | ZNF263 | MA0528.1 | chr11:17008941-17008962 | GCTCCCTCCTTTTCCTCCTTA | - | 6.37 | ZNF740 | MA0753.2 | chr11:17008805-17008818 | CCACACCCCCCAC | + | 6.03 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23209 | chr11:17006345-17010079 | Colon_Crypt_1 | SE_24588 | chr11:17006954-17010047 | Colon_Crypt_2 | SE_27642 | chr11:17005603-17011510 | Fetal_Intestine | SE_28618 | chr11:17005858-17011943 | Fetal_Intestine_Large | SE_31464 | chr11:17005871-17010093 | Gastric | SE_42048 | chr11:17006935-17008802 | LNCaP | SE_42048 | chr11:17008809-17010048 | LNCaP | SE_48027 | chr11:17007452-17009993 | Pancreas | SE_50712 | chr11:17006304-17010109 | Sigmoid_Colon | SE_52571 | chr11:17006346-17010116 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I016978 | chr11 | 17000394 | 17011590 |
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Enhancer Sequence | AGTGTGTTCA GGCCAGAGGG GAATGGTGTG CTTTAACAGG ACACAGACAC AGGAAGAGAA 60 GCCCAAGTCA GGACACCTCT GAAGGCCCTC ATCAGGAAGC ATATCAGGAT GAGGTATTTG 120 GGCCCCTGTA GGGAGAACAG GATGGAGGCA AGAAAACCAG TCGGAACCAT CTGCACCGCT 180 GCAGATATGA GTTGGTGACA GTGGGGTCTT TAGGAGGCAC CAGAGAAAGG ACTAATCACA 240 AGAATCTGTT ACAAATCACA GGTGCAAGAC CCCATGGAGA AGGGAGGCAT CGAATGAGCC 300 CAGACACATT TTGAGTACAT AAGAAAAGTG CAGCCCCACC AGAGCCCTCC TGGGAATGCT 360 GCAAAGCTGC TGGGGAGATG CCAGCAGAAC CATGTCACAC CTTGCCCACA GTCACCAAAG 420 TGGGGACCCT ACTGACTGGC TGGAGGCAAG GAGGAAGTCA GGGGAGAGAA ACCATAAAAA 480 TTGCTCACTA TTTATTTCAC TTTCACTTTG AGCACACAAG TGGGGAGAAG ACGCCCTGGC 540 CCAGGAGTAG AGAAACCTGG CTGGAGTCCC AGCTGTCACC AACAACCTGA GTAACCTTGG 600 GCAGGTGACT TCACCGCTGG GGCTCAGCTT CCCCATCTAT AAACCAGAGC TTCCACCATG 660 AGCCCCACCT CTACCAACAT CCTGGAAAGG CCCCAATCAG ATAAGTATCA GCTCTGCATA 720 GCTTTATGTA GCACCTACTA TATGATCTTC CTTGTACCAG GAAGGGAGGC AGGAAAGGGG 780 CAGGCCGAGC CCCTGCCCAG AGAAGGTTTT AACAAGGTGG TCCAAGCAGG TACTGCAGAA 840 CACCGGCAAG GGCATTTCCA GCCACATTCT CCAGCCAGTC TTACTGCCCA GCCCAACCCA 900 GCCCAGGGAA GGCGGAGAGG AAGCAGTGAG CTGTTTTACA ATCCATCAAA TTAATTGCCC 960 CAAATGGGAA ATTTGCAGGC CTCCTACAGC CTCCTGTGTA TTCCATAATC TCCCATGGCC 1020 CTAATCTGCT GAGAAAGAAT GTGTGGGCTG TAATCTTTTC AGCCCACTGT TCACAGGGGC 1080 AATGCCTTGG AAAAACCTCA GTCCCCACCA GTGATCACTC CCTCCCAACC AAAAGCCTCC 1140 CCGACCTCCC ATCCCCCACA CCCCCCACTG ACCTGGTGGC CAGCCAAGGC CTGGCTCCGC 1200 CCCCCAGAAG CCAGCTAGGC CAACCTTGGC CTTGACTTTG ACCTCGGAAA GGAGACCTGC 1260 CCAACCAGCT CCTTTGGTAA ATACAACTTT TGCTCCCTCC TTTTCCTCCT TAAGACAGAA 1320 CAGCCTGGCA GGAGGCAGAA CCAGGAGAAA TGGCTTCCGA GTAGAGACGC ACCCTTGAGG 1380 CGTGGTGAAA ACAGCCCCAG GTGAGGTGCT GGGCATTGGT TCTAACCTTT GCTTACCCTA 1440 TCCCTGCTAG GAAACCCACT TCCCATCTCT GGACCTCATC TTCATTTGAG AAATGAAGGG 1500 AATGTAAAAC AGCCTCCCAG GAACTCCTTA CCCCACCCCT TTAAACAAGT TGCTTCTTTG 1560 CTTCTGCTGT AACCTTTGCC TGCTCCTTTT CCTGCATAAT GAAGCCTCTG TCTAGGCCCA 1620 ACTCAAATGT CACTTTCCCC ACGAAGGCTT CCTGGATCCC TCCCTTCTCA ACACCTGTCC 1680 CAAACTCTTT 1690
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