| Tag | Content |
|---|
EnhancerAtlas ID | HS105-25824 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr14:100658570-100660010 |
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 | AATTAATCAA GGTCGGCCTT CCATCAAGGT CGGCTTCTCG GCTCCCCAGC CCCCGCGCCT 60
CACGGGGACC TCAGGCCTCG GCAGGGTCCT CTCCCTTTGC ATCTCCTACT AGTCAGCTGT 120
CGGTGGTGAT GGCCCGTGCC AAGTTCACGG TCTCAGCCTG ACGAAAGGCG GCCTTTACCA 180
GCCTCAGGAC CCCCAACGAA CCTGGGGCCA TGGCTGGGGA GGGGGCTCTG CCCAGGCTCT 240
GCGTTCTGGG ACAGGGGTCC CCAGATGGCC ATGCGTCAAG GCCCAGGGAC CTGTTTGTGG 300
GCCCGAGAGC ACGGGGGTCA GGGGTGGGGC TCGAGTCTCG TCCCAGGGCT CCGGGACAAG 360
CTTCCTGGAG GAGGCAGCGT GAGCTCTGGG AGGTAGAGGT CAAGACCTCA AAAAATGGGG 420
GGACATGGGC GGAGGGGGCA TTTTGTAACT CCTACGTCCC TGCAGAAGCC CAGACCCTCA 480
GAGACTAGGA ACTGAGGCCT GGCAGAGTGG GGTGGGCCAG CAATCACGCG CCAGGCCACA 540
CGAGGAGAGC CCACTGCCCC GGGGATGTCA GACGCGGGGC GGCCTCGGCG ACCGCACACG 600
CCATAGAAAG GTCACCGAAC TTGGCCGCCC GGCCGTCCCG GAAATCGCTA CTGCCCGGCA 660
GCCCTGGGGC CTCCACAACC GCGTCCCGGC GGCTCAAGTT GCCCTTTGTC GCCCCCTGCC 720
GACCAGTCTC CCTGCGGCTC CCGCGCGGGA CAATCAGGCG GGCCGGGCTC GGAAATAGTG 780
GGCATGGGTC CCTGAGGCGC GGGGATTGGC CGCTCTGTGT CATGTGTCCT CGGCTCGGGC 840
CAACCAGCGA GGGAGGCAAA GTCCCATCCC GCGCGTCCCG TAGCCCTTCA GCGAGCTGTG 900
GGCGGGGCGT CAGGCCTGAC ACCTCGGCCA GAGGGCGGGG CCGGAGACCT GAGCGGCGCC 960
GCTTCCGCTC TTTCGCCCAG GTGCCTTGGA GCCGCTGCTC TCGCCTCCCT TCTCCACCTA 1020
GCGGCGGTGT TTCACACCCC GGAGTGGCTT TTTGGGGATA AAGGCACAAA TCTTTGCCAG 1080
ACCTCCCGCC AGGCCCCCTG GCCTGCCACG TGCTCCTTGC CGGCCTAGAC TCACCCAGGC 1140
TGTGCCCTCT GCTCAGAACG ACCTTTCCCC CCTTCCTCTC CCCCTCGCTT GCTCCGACTG 1200
TTCTTTGCAA TCCCGGCTGG GGTTGGGTTA AGGGCCTTCT GGGGCTTCTT CATACCCTGT 1260
GCATCTTCCT CCTACTGGCA CCGACCACCC CACACTGGGC TGCCATCTGC TTGTCTACAC 1320
CCACTGACTT TTCATCTCTG TATCTCCCCA GTAAGCAGGA GTGGCTCACA GAAGGCACGT 1380
TAATACCTGT GTGTTAATAT AAACCAAGGA GCGGGACGAT AGCTAGGAAG TAACATCCCT 1440
|
