| Tag | Content |
|---|
EnhancerAtlas ID | HS195-02087 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr14:100658670-100659900 |
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 |
|
| | 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 | ATCTCCTACT AGTCAGCTGT CGGTGGTGAT GGCCCGTGCC AAGTTCACGG TCTCAGCCTG 60
ACGAAAGGCG GCCTTTACCA GCCTCAGGAC CCCCAACGAA CCTGGGGCCA TGGCTGGGGA 120
GGGGGCTCTG CCCAGGCTCT GCGTTCTGGG ACAGGGGTCC CCAGATGGCC ATGCGTCAAG 180
GCCCAGGGAC CTGTTTGTGG GCCCGAGAGC ACGGGGGTCA GGGGTGGGGC TCGAGTCTCG 240
TCCCAGGGCT CCGGGACAAG CTTCCTGGAG GAGGCAGCGT GAGCTCTGGG AGGTAGAGGT 300
CAAGACCTCA AAAAATGGGG GGACATGGGC GGAGGGGGCA TTTTGTAACT CCTACGTCCC 360
TGCAGAAGCC CAGACCCTCA GAGACTAGGA ACTGAGGCCT GGCAGAGTGG GGTGGGCCAG 420
CAATCACGCG CCAGGCCACA CGAGGAGAGC CCACTGCCCC GGGGATGTCA GACGCGGGGC 480
GGCCTCGGCG ACCGCACACG CCATAGAAAG GTCACCGAAC TTGGCCGCCC GGCCGTCCCG 540
GAAATCGCTA CTGCCCGGCA GCCCTGGGGC CTCCACAACC GCGTCCCGGC GGCTCAAGTT 600
GCCCTTTGTC GCCCCCTGCC GACCAGTCTC CCTGCGGCTC CCGCGCGGGA CAATCAGGCG 660
GGCCGGGCTC GGAAATAGTG GGCATGGGTC CCTGAGGCGC GGGGATTGGC CGCTCTGTGT 720
CATGTGTCCT CGGCTCGGGC CAACCAGCGA GGGAGGCAAA GTCCCATCCC GCGCGTCCCG 780
TAGCCCTTCA GCGAGCTGTG GGCGGGGCGT CAGGCCTGAC ACCTCGGCCA GAGGGCGGGG 840
CCGGAGACCT GAGCGGCGCC GCTTCCGCTC TTTCGCCCAG GTGCCTTGGA GCCGCTGCTC 900
TCGCCTCCCT TCTCCACCTA GCGGCGGTGT TTCACACCCC GGAGTGGCTT TTTGGGGATA 960
AAGGCACAAA TCTTTGCCAG ACCTCCCGCC AGGCCCCCTG GCCTGCCACG TGCTCCTTGC 1020
CGGCCTAGAC TCACCCAGGC TGTGCCCTCT GCTCAGAACG ACCTTTCCCC CCTTCCTCTC 1080
CCCCTCGCTT GCTCCGACTG TTCTTTGCAA TCCCGGCTGG GGTTGGGTTA AGGGCCTTCT 1140
GGGGCTTCTT CATACCCTGT GCATCTTCCT CCTACTGGCA CCGACCACCC CACACTGGGC 1200
TGCCATCTGC TTGTCTACAC CCACTGACTT 1230
|
