Tag | Content |
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EnhancerAtlas ID | HS098-18483 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr14:100658510-100660070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr14:100659731-100659752 | CCTTTCCCCCCTTCCTCTCCC | - | 6.21 | ZNF263 | MA0528.1 | chr14:100659733-100659754 | TTTCCCCCCTTCCTCTCCCCC | - | 6.41 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23822 | chr14:100658575-100659390 | Colon_Crypt_2 | SE_23822 | chr14:100659435-100660335 | Colon_Crypt_2 | SE_24776 | chr14:100658405-100660543 | Colon_Crypt_3 | SE_27982 | chr14:100658545-100660323 | Fetal_Intestine | SE_29025 | chr14:100658411-100660318 | Fetal_Intestine_Large | SE_31574 | chr14:100658310-100661006 | Gastric | SE_35748 | chr14:100658539-100659393 | HepG2 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I100192 | chr14 | 100658488 | 100660354 |
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Enhancer Sequence | GAAAAAAAAA AAGAAAAGAA AAAAAAGATA AAGAAATAAA TTTCTTCTGC CAGATACCTT 60 AATTAATCAA GGTCGGCCTT CCATCAAGGT CGGCTTCTCG GCTCCCCAGC CCCCGCGCCT 120 CACGGGGACC TCAGGCCTCG GCAGGGTCCT CTCCCTTTGC ATCTCCTACT AGTCAGCTGT 180 CGGTGGTGAT GGCCCGTGCC AAGTTCACGG TCTCAGCCTG ACGAAAGGCG GCCTTTACCA 240 GCCTCAGGAC CCCCAACGAA CCTGGGGCCA TGGCTGGGGA GGGGGCTCTG CCCAGGCTCT 300 GCGTTCTGGG ACAGGGGTCC CCAGATGGCC ATGCGTCAAG GCCCAGGGAC CTGTTTGTGG 360 GCCCGAGAGC ACGGGGGTCA GGGGTGGGGC TCGAGTCTCG TCCCAGGGCT CCGGGACAAG 420 CTTCCTGGAG GAGGCAGCGT GAGCTCTGGG AGGTAGAGGT CAAGACCTCA AAAAATGGGG 480 GGACATGGGC GGAGGGGGCA TTTTGTAACT CCTACGTCCC TGCAGAAGCC CAGACCCTCA 540 GAGACTAGGA ACTGAGGCCT GGCAGAGTGG GGTGGGCCAG CAATCACGCG CCAGGCCACA 600 CGAGGAGAGC CCACTGCCCC GGGGATGTCA GACGCGGGGC GGCCTCGGCG ACCGCACACG 660 CCATAGAAAG GTCACCGAAC TTGGCCGCCC GGCCGTCCCG GAAATCGCTA CTGCCCGGCA 720 GCCCTGGGGC CTCCACAACC GCGTCCCGGC GGCTCAAGTT GCCCTTTGTC GCCCCCTGCC 780 GACCAGTCTC CCTGCGGCTC CCGCGCGGGA CAATCAGGCG GGCCGGGCTC GGAAATAGTG 840 GGCATGGGTC CCTGAGGCGC GGGGATTGGC CGCTCTGTGT CATGTGTCCT CGGCTCGGGC 900 CAACCAGCGA GGGAGGCAAA GTCCCATCCC GCGCGTCCCG TAGCCCTTCA GCGAGCTGTG 960 GGCGGGGCGT CAGGCCTGAC ACCTCGGCCA GAGGGCGGGG CCGGAGACCT GAGCGGCGCC 1020 GCTTCCGCTC TTTCGCCCAG GTGCCTTGGA GCCGCTGCTC TCGCCTCCCT TCTCCACCTA 1080 GCGGCGGTGT TTCACACCCC GGAGTGGCTT TTTGGGGATA AAGGCACAAA TCTTTGCCAG 1140 ACCTCCCGCC AGGCCCCCTG GCCTGCCACG TGCTCCTTGC CGGCCTAGAC TCACCCAGGC 1200 TGTGCCCTCT GCTCAGAACG ACCTTTCCCC CCTTCCTCTC CCCCTCGCTT GCTCCGACTG 1260 TTCTTTGCAA TCCCGGCTGG GGTTGGGTTA AGGGCCTTCT GGGGCTTCTT CATACCCTGT 1320 GCATCTTCCT CCTACTGGCA CCGACCACCC CACACTGGGC TGCCATCTGC TTGTCTACAC 1380 CCACTGACTT TTCATCTCTG TATCTCCCCA GTAAGCAGGA GTGGCTCACA GAAGGCACGT 1440 TAATACCTGT GTGTTAATAT AAACCAAGGA GCGGGACGAT AGCTAGGAAG TAACATCCCT 1500 GGGCATCATC TGAGTACCAG GCCCCCTGCC AGGTACTTTA GAGGCTACTT GATGTTCAGG 1560
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