| Tag | Content |
|---|
EnhancerAtlas ID | HS069-02666 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr14:100658240-100660480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr14:100660295-100660315 | GGGGTGGGGGTGGGGGTGGG | - | 6.27 | | RREB1 | MA0073.1 | chr14:100658428-100658448 | CCACCACCCACCCACTTCCG | + | 6.57 | | RREB1 | MA0073.1 | chr14:100658424-100658444 | CCCCCCACCACCCACCCACT | + | 7.63 | | ZNF263 | MA0528.1 | chr14:100659731-100659752 | CCTTTCCCCCCTTCCTCTCCC | - | 6.21 | | ZNF263 | MA0528.1 | chr14:100659733-100659754 | TTTCCCCCCTTCCTCTCCCCC | - | 6.41 |
|
| | 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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I100192 | chr14 | 100658488 | 100660354 |
|
Enhancer Sequence | TCTCTGGGAG AGGCTATCAC CAAGATAAAT CGGTAAGGCT TAATTCCATG TCCAGTGTTT 60
TTGGCAAAAC CCTTGTTCCC GAGGGGGTGA GTGGCCTTCC CAGCAGGCTC TGCTGAATTC 120
TGGAAGAGCC TGTTTCCAGA AACTTTGTTT TGTACATGTC TTGGCAAATG ATCACCACCC 180
CCCTCCCCCC ACCACCCACC CACTTCCGAA GTGGTCTAGG GCTTAAGTCC AGATGCGGAT 240
GGGCTCAGGG CGGGGTGGGA GAAGTCAGGG GAAAAAAAAA AAGAAAAGAA AAAAAAGATA 300
AAGAAATAAA TTTCTTCTGC CAGATACCTT AATTAATCAA GGTCGGCCTT CCATCAAGGT 360
CGGCTTCTCG GCTCCCCAGC CCCCGCGCCT CACGGGGACC TCAGGCCTCG GCAGGGTCCT 420
CTCCCTTTGC ATCTCCTACT AGTCAGCTGT CGGTGGTGAT GGCCCGTGCC AAGTTCACGG 480
TCTCAGCCTG ACGAAAGGCG GCCTTTACCA GCCTCAGGAC CCCCAACGAA CCTGGGGCCA 540
TGGCTGGGGA GGGGGCTCTG CCCAGGCTCT GCGTTCTGGG ACAGGGGTCC CCAGATGGCC 600
ATGCGTCAAG GCCCAGGGAC CTGTTTGTGG GCCCGAGAGC ACGGGGGTCA GGGGTGGGGC 660
TCGAGTCTCG TCCCAGGGCT CCGGGACAAG CTTCCTGGAG GAGGCAGCGT GAGCTCTGGG 720
AGGTAGAGGT CAAGACCTCA AAAAATGGGG GGACATGGGC GGAGGGGGCA TTTTGTAACT 780
CCTACGTCCC TGCAGAAGCC CAGACCCTCA GAGACTAGGA ACTGAGGCCT GGCAGAGTGG 840
GGTGGGCCAG CAATCACGCG CCAGGCCACA CGAGGAGAGC CCACTGCCCC GGGGATGTCA 900
GACGCGGGGC GGCCTCGGCG ACCGCACACG CCATAGAAAG GTCACCGAAC TTGGCCGCCC 960
GGCCGTCCCG GAAATCGCTA CTGCCCGGCA GCCCTGGGGC CTCCACAACC GCGTCCCGGC 1020
GGCTCAAGTT GCCCTTTGTC GCCCCCTGCC GACCAGTCTC CCTGCGGCTC CCGCGCGGGA 1080
CAATCAGGCG GGCCGGGCTC GGAAATAGTG GGCATGGGTC CCTGAGGCGC GGGGATTGGC 1140
CGCTCTGTGT CATGTGTCCT CGGCTCGGGC CAACCAGCGA GGGAGGCAAA GTCCCATCCC 1200
GCGCGTCCCG TAGCCCTTCA GCGAGCTGTG GGCGGGGCGT CAGGCCTGAC ACCTCGGCCA 1260
GAGGGCGGGG CCGGAGACCT GAGCGGCGCC GCTTCCGCTC TTTCGCCCAG GTGCCTTGGA 1320
GCCGCTGCTC TCGCCTCCCT TCTCCACCTA GCGGCGGTGT TTCACACCCC GGAGTGGCTT 1380
TTTGGGGATA AAGGCACAAA TCTTTGCCAG ACCTCCCGCC AGGCCCCCTG GCCTGCCACG 1440
TGCTCCTTGC CGGCCTAGAC TCACCCAGGC TGTGCCCTCT GCTCAGAACG ACCTTTCCCC 1500
CCTTCCTCTC CCCCTCGCTT GCTCCGACTG TTCTTTGCAA TCCCGGCTGG GGTTGGGTTA 1560
AGGGCCTTCT GGGGCTTCTT CATACCCTGT GCATCTTCCT CCTACTGGCA CCGACCACCC 1620
CACACTGGGC TGCCATCTGC TTGTCTACAC CCACTGACTT TTCATCTCTG TATCTCCCCA 1680
GTAAGCAGGA GTGGCTCACA GAAGGCACGT TAATACCTGT GTGTTAATAT AAACCAAGGA 1740
GCGGGACGAT AGCTAGGAAG TAACATCCCT GGGCATCATC TGAGTACCAG GCCCCCTGCC 1800
AGGTACTTTA GAGGCTACTT GATGTTCAGG CCCATGGCAG CCCTGGGAGG GAGGCACAAA 1860
GGCTCTTTTG TTCCTGGGGA GTCAGTGGAG GCCCCTAGAG GCTGAATGAC TGTCTGGGTC 1920
CCCCAGCTGG ACTGTTTGGG GACAGGCCTG GGGAGCTGAG GGCACCCTCA TACCAGGCAG 1980
CCTTGCGCCT GAAGCTCTGC TGGTGAAAAC TGATGGGCAG GGCCCTGGAA GGGAGAGTCA 2040
GCGCCTGCGG GGGCGGGGGT GGGGGTGGGG GTGGGAAGGC AAGCGGAGGG GAAAGGTGAG 2100
CATAGACAGG CATTTGTGAT GGCCACAGGC CTTCACTGCT ACCCTGACAT CAGGGCCAAT 2160
GGCAACCTGC AAGGCCCTTC AAAGCCCTGC TTCCACCTCT GCCCATCTCT GGCTGCAACC 2220
TCCTGGTTCT CCCACCCTGT 2240
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