| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00122 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:2342350-2343820 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr1:2342915-2342929 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_24340 | chr1:2343111-2346064 | Colon_Crypt_2 | | SE_25169 | chr1:2343208-2346524 | Colon_Crypt_3 | | SE_27514 | chr1:2343120-2346479 | Esophagus | | SE_41711 | chr1:2339731-2342704 | LNCaP | | SE_41711 | chr1:2342986-2346400 | LNCaP |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I002408 | chr1 | 2339732 | 2342704 |
|
Enhancer Sequence | GGGAACAGTG TCTGGCACAG GGGTAAGTGC CAAGTGTACT GTAAAACAAG TAAGTACACA 60
CACAAAAAAT TCTCATCATG TCACTCTCCT GTTCAGAATC CACCAATGGC TGCCCACCTG 120
ACACCCATGG GCCTCCCGGC ACGGAGCCTG GCTGTCCTCT GATATTTACC CATGCTCTTC 180
CTGTCCCATG GCACTGTTCC TTTGGCCACG ACACCCCCAC CACTGGGCTC TAGTGCCACT 240
GCTCCCTGAA ACGTTCTGCT GGGAGTTCAT GCCTTTAACG ACTGCCTGCC CCACCCCCCA 300
AAGACTTGAT GGCTTTGCCT TTTTTTTTTT TTTTTTTTTT TTGAGATGGA GTCTCACTCT 360
GTTGCCCAGA CTGGAGTGCA GTGGCACGAT CTTGGCTTAC TGCAACCTCC GCCTCCCGGG 420
TTCAAGTGAT TCTGTCTCAG CCTCCCAAGT AGCTGGGATT ACACGCACGC GCCACCACGC 480
CCTGCTGATT TTTGTATTTT TAGTAGAGAC GGGGTTTCAC CATGTTGTGT AGACTGGTCT 540
CGAACTCCTG ACCTCAAGTG ATCCACCCGC CTCGGCCTCC CAAAGTGCTG GGATTACAGG 600
CGTGAGCCAC CACACCCGGC ATCTTTTTTT TTTCGTTTTT TAATCGGTGA TGGGGTCTGG 660
CCCCGTCGCC CAGGCTGGAG TGCAGCGGCA CAATCATGGC TCACTGCAGC CTCATCCCTC 720
GGGCTCAGGC GATTCTCTTG CCTCAGCCTC CTGAAGAGCT GGGATTACAG ACGCCGCCAC 780
CACGTCCGGC TAATTTTCAG ATTTTTTGTA GAGACGGGGT CTTGCCATGT TGCCCAGGCT 840
GGTTTCAAAC TCCTGGGCTC AAGCGATCCT CCCGCCTCTG CCTCCCAAAC TGCTGGGATG 900
ACAGGTGCTG CTTCATTGAG TACACTGGCT TCTGTACTCA GCTCCCGGCC TGGTGAGGCA 960
GGCAGGGCCT GGCTGAGCCT ACACTGGGGT CAGCAGGGCG AGGGGCCTGG GCTGCTGCTC 1020
AGGCCTAGGA AAGGCCGGGG TCAGTGTGAA CCGGACCGAG GTATGAGGCG TTCGCGCCGC 1080
GGGCGCTCTG ACCCCTCTGC TCACAGGGGA GGATCGGAGG GAGGCTTGAA GCACTTGCCA 1140
AGGCCTCACA CCTGGAGGGG ACAGAGTCTT CCCCAGCCGC TGGCGTCAGC TGGACCTGCC 1200
CTGAGCTGGG GACGGGAAGG GCTTGGGCGG GAACTGGAGG CCCACGCAGG TCCCCCGCGG 1260
TGTCTGCGGC CTGTGCCTCT GGGGCCACCT GGCCAGGGAG GGCAGGAGGT GCCCCGCACA 1320
TCCCTGAATG GCCGCAGGGC AGGCGAAGGA GACTGCCGGG TCCCAGGTTG TGGGACGGGC 1380
CCAGGCGACC GTGACCACAC ACGGCAGACA CCCCGCCTCC ATGAGGGGCA ACACCCCCTG 1440
GGCCGCTCGC GAGGACGTCC GGCCGCGCCC 1470
|
