Tag | Content |
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EnhancerAtlas ID | HS028-00785 |
Organism | Homo sapiens |
Tissue/cell | Colo829 |
Coordinate | chr12:13052430-13053520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr12:13053459-13053480 | CTCCTCTTCCTTTCCTCCCTC | - | 6.43 | ZNF263 | MA0528.1 | chr12:13053499-13053520 | TCCCTTCCCTCTCCCTCTTCC | - | 6.4 | ZNF263 | MA0528.1 | chr12:13053466-13053487 | TCCTTTCCTCCCTCTTCCTCT | - | 6.5 | ZNF263 | MA0528.1 | chr12:13053206-13053227 | GAATGAGGATGAGGGGGAGAA | + | 6.78 | ZNF263 | MA0528.1 | chr12:13053212-13053233 | GGATGAGGGGGAGAAAGAAAG | + | 6.81 | ZNF263 | MA0528.1 | chr12:13053463-13053484 | TCTTCCTTTCCTCCCTCTTCC | - | 6.92 | ZNF263 | MA0528.1 | chr12:13053209-13053230 | TGAGGATGAGGGGGAGAAAGA | + | 7.14 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_02173 | chr12:13051911-13053728 | Aorta | SE_23547 | chr12:13052684-13053623 | Colon_Crypt_1 | SE_28138 | chr12:13052808-13053649 | Fetal_Intestine | SE_28922 | chr12:13051231-13057938 | Fetal_Intestine_Large | SE_34394 | chr12:13052411-13053680 | HCT-116 | SE_36163 | chr12:13051744-13055812 | HMEC | SE_38847 | chr12:13051287-13055917 | HUVEC | SE_57272 | chr12:13050050-13053678 | VACO_400 | SE_58021 | chr12:13052873-13053228 | VACO_9m | SE_64427 | chr12:13051485-13053710 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I012897 | chr12 | 13050309 | 13057779 |
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Enhancer Sequence | GAGCTATTCT TTCTGACCAT GTGACACTGG ACATGTACCT TCCTCACTCT GTTAGGTTTC 60 TCACCTATAA AATGGGCTGT AGGAATGTTA AATGAGGTAA TGGATGTAAA AGCATGTAAA 120 TGAGAGAATA TGTGTAAAAA TACATAACTA CTCAGCATAG TGCCTGACTC ATAATAGGAC 180 TCAGGAGGTG ACAGTAGCTG TCATTATTCT TACTCATAAT TACATCATGA CTGTTATTAC 240 TACTGACTGA ATGTAGCAAT TCGAGAATAG AGAAAAAATG AAAATGCTAG AAAGTCACAC 300 ATTTTCAGGG CTGGGCTGGC GCGAAGACAC ATTTTGACAG AATGAGAGAA ATCTCATAGG 360 AAGGAAGACA AAGTCAGTTT GTCTTTGCAA GGTTCTGGGC CCCAGATGAT TCATTCTCAG 420 ATGCTCTGGG AAGGACTGCG TAGAATAAGC ATGGGCAAAC TTCCAGGCCT AGTCACAAGC 480 AACTCTACAC ACTTTCCCCA TCTCTCTGGT TGCGAAGAGG AGTCTCAGGT TAGAAACCCA 540 AAGCGGGAGA CTCATCACAT GTTCACGTTT TTCCCTGCAC AGTGGTCAGT GCTGTGTGTC 600 AGTCAAGGCC ATGTCTAGGG TCAGCGCTGC TCCAGGAGCC TCTGGCTTTG TCCTTCAGGT 660 GGGCAGTCCC TTGCTGTGTC TCTTCTTCAG ACCCTTCAAC CTTACCTCTA GCCCTGGCTT 720 TTAGTTTGGG TAGGAGTTTG TGGCACATAC TCTTTTAATG ACAGGAGATG GGGCAAGAAT 780 GAGGATGAGG GGGAGAAAGA AAGACATCTG GAAGTTTTGT ACATGAAGCT CCCCAGGTGG 840 GTGAACGGTG GAGCTGAACA TGAGTTCAGA CCACGTAGTT CAGCAGCGTG TCCTGCATTT 900 TATAGATGAG AGGAGGCTTT GAGAGGTCAA GTGACTTACT TGTTCACACA GCCTGGCAGC 960 TGAAACCCCT TCTCCCTAAA GGGGAGGAGG AACAGAGGGC TTGGAGTTGA CCCAAGAAAT 1020 GACTTCGCCC TCCTCTTCCT TTCCTCCCTC TTCCTCTTGT TCTTATTCTT CCCTTCCCTC 1080 TCCCTCTTCC 1090
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