Tag | Content |
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EnhancerAtlas ID | HS098-34266 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr20:17854370-17855190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr20:17855039-17855059 | GCCCCACCCACCCACACACT | + | 6.19 | SP2 | MA0516.2 | chr20:17855035-17855052 | CAAAGCCCCACCCACCC | + | 6.13 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23578 | chr20:17852942-17858143 | Colon_Crypt_1 | SE_24205 | chr20:17853643-17856102 | Colon_Crypt_2 | SE_28415 | chr20:17853999-17857306 | Fetal_Intestine | SE_29297 | chr20:17854017-17858372 | Fetal_Intestine_Large | SE_35399 | chr20:17853218-17860231 | HepG2 | SE_50301 | chr20:17852649-17858273 | Sigmoid_Colon | SE_52789 | chr20:17853333-17857202 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I017872 | chr20 | 17853493 | 17858320 |
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Enhancer Sequence | GGATCCTGAA TCCTAGCTAT CCCTTCAGAG CCACCCCTCT GGCTTCCAAG CACCTGCACT 60 ACCCACTCCC ACCCCTCCCT GGAAGGGATG GCGCAGCCTG GGAGCCAGCT GCTCTGGGGG 120 GCTCAGACCT GTGGGCTGGA TTGTCCATGT GTCAGGGAAG GAAAGGGAAG CCCATGGCAG 180 GAGGGACACC CTCTTATGGG TGGTAGCAAC TCCATGGAGC CCAGGCTGCA TCGTTCACTG 240 AGGCTGCTAA TGTTTGAACC TATCTTTGAA TAAGATCCAC CCTCTTGCAC TGGCAAGTCC 300 AAGCTGTAGT AAACCCTGAG GGAGACCCAC AGTCCAGCTG CAAGGCCCTG CCCCACTCTT 360 GGCCGCTGGC AGAAGCTCCA GGCTTGCCGA GGGGTGCCAC GTAGCAGAGG CAGTCTCCGC 420 CTCTAGCCCA TCCCACTCCT TCATCTGCTT CTCGTTAGCT TCAAAAGTAA GGCCTGGCGC 480 TGTGCCCTGG GCAGGAGGGA GAGCTTGGTG TGGCCGCTCA GAGCTTCACC TCCCTTGCCT 540 GGGGTTTCTC TTCTCCTGCC CCATCCATCG TCAGCACAGC TGACTGCTTC TGGGGCTCCT 600 CTGTCTACCT TCCCCACGTT CCAGCACCCC CCTTCCCCTG CCCCTCTGTA GCAACCGCCT 660 CCCTGCAAAG CCCCACCCAC CCACACACTC ATACACACAC CCCTCTCACT CCCCTGGCAC 720 TCAGTCCCTC CAAGCTTCCT TCCTTATCCC TTTAGAGCCC TGCAGCCCTC AGGCAGTGTA 780 GCCCAGAGGT TCAAGGGCAT TCGCTCTGGT ATCAGAAGGG 820
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