| Tag | Content |
|---|
EnhancerAtlas ID | HS184-10753 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr14:100658590-100660350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr14:100660295-100660315 | GGGGTGGGGGTGGGGGTGGG | - | 6.27 | | 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 | CCATCAAGGT CGGCTTCTCG GCTCCCCAGC CCCCGCGCCT CACGGGGACC TCAGGCCTCG 60
GCAGGGTCCT CTCCCTTTGC ATCTCCTACT AGTCAGCTGT CGGTGGTGAT GGCCCGTGCC 120
AAGTTCACGG TCTCAGCCTG ACGAAAGGCG GCCTTTACCA GCCTCAGGAC CCCCAACGAA 180
CCTGGGGCCA TGGCTGGGGA GGGGGCTCTG CCCAGGCTCT GCGTTCTGGG ACAGGGGTCC 240
CCAGATGGCC ATGCGTCAAG GCCCAGGGAC CTGTTTGTGG GCCCGAGAGC ACGGGGGTCA 300
GGGGTGGGGC TCGAGTCTCG TCCCAGGGCT CCGGGACAAG CTTCCTGGAG GAGGCAGCGT 360
GAGCTCTGGG AGGTAGAGGT CAAGACCTCA AAAAATGGGG GGACATGGGC GGAGGGGGCA 420
TTTTGTAACT CCTACGTCCC TGCAGAAGCC CAGACCCTCA GAGACTAGGA ACTGAGGCCT 480
GGCAGAGTGG GGTGGGCCAG CAATCACGCG CCAGGCCACA CGAGGAGAGC CCACTGCCCC 540
GGGGATGTCA GACGCGGGGC GGCCTCGGCG ACCGCACACG CCATAGAAAG GTCACCGAAC 600
TTGGCCGCCC GGCCGTCCCG GAAATCGCTA CTGCCCGGCA GCCCTGGGGC CTCCACAACC 660
GCGTCCCGGC GGCTCAAGTT GCCCTTTGTC GCCCCCTGCC GACCAGTCTC CCTGCGGCTC 720
CCGCGCGGGA CAATCAGGCG GGCCGGGCTC GGAAATAGTG GGCATGGGTC CCTGAGGCGC 780
GGGGATTGGC CGCTCTGTGT CATGTGTCCT CGGCTCGGGC CAACCAGCGA GGGAGGCAAA 840
GTCCCATCCC GCGCGTCCCG TAGCCCTTCA GCGAGCTGTG GGCGGGGCGT CAGGCCTGAC 900
ACCTCGGCCA GAGGGCGGGG CCGGAGACCT GAGCGGCGCC GCTTCCGCTC TTTCGCCCAG 960
GTGCCTTGGA GCCGCTGCTC TCGCCTCCCT TCTCCACCTA GCGGCGGTGT TTCACACCCC 1020
GGAGTGGCTT TTTGGGGATA AAGGCACAAA TCTTTGCCAG ACCTCCCGCC AGGCCCCCTG 1080
GCCTGCCACG TGCTCCTTGC CGGCCTAGAC TCACCCAGGC TGTGCCCTCT GCTCAGAACG 1140
ACCTTTCCCC CCTTCCTCTC CCCCTCGCTT GCTCCGACTG TTCTTTGCAA TCCCGGCTGG 1200
GGTTGGGTTA AGGGCCTTCT GGGGCTTCTT CATACCCTGT GCATCTTCCT CCTACTGGCA 1260
CCGACCACCC CACACTGGGC TGCCATCTGC TTGTCTACAC CCACTGACTT TTCATCTCTG 1320
TATCTCCCCA GTAAGCAGGA GTGGCTCACA GAAGGCACGT TAATACCTGT GTGTTAATAT 1380
AAACCAAGGA GCGGGACGAT AGCTAGGAAG TAACATCCCT GGGCATCATC TGAGTACCAG 1440
GCCCCCTGCC AGGTACTTTA GAGGCTACTT GATGTTCAGG CCCATGGCAG CCCTGGGAGG 1500
GAGGCACAAA GGCTCTTTTG TTCCTGGGGA GTCAGTGGAG GCCCCTAGAG GCTGAATGAC 1560
TGTCTGGGTC CCCCAGCTGG ACTGTTTGGG GACAGGCCTG GGGAGCTGAG GGCACCCTCA 1620
TACCAGGCAG CCTTGCGCCT GAAGCTCTGC TGGTGAAAAC TGATGGGCAG GGCCCTGGAA 1680
GGGAGAGTCA GCGCCTGCGG GGGCGGGGGT GGGGGTGGGG GTGGGAAGGC AAGCGGAGGG 1740
GAAAGGTGAG CATAGACAGG 1760
|
