| Tag | Content |
|---|
EnhancerAtlas ID | HS050-19434 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr13:106643880-106644670 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr13:106644268-106644278 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr13:106644268-106644278 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr13:106644268-106644278 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr13:106644268-106644278 | AACAGCTGTT | - | 6.02 | | NFIC | MA0161.2 | chr13:106644247-106644258 | TCTGCCAAGAA | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34149 | chr13:106642640-106645099 | HCC1954 | | SE_36583 | chr13:106641912-106645243 | HMEC |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I105989 | chr13 | 106642150 | 106644938 |
|
Enhancer Sequence | CTTACTATCT TAACACAGTT CCTCACCATT CTTTTCTTAA ATAATTGGTT TCTCAGCTGG 60
TCTTTTGACT CATGTCTTTC CAACCCATTC TCTGCCTGGT ACAAAAGTCA CTTTCCAAAC 120
ACAAGTCTGA TCATGCTGAC CCTGACTGAG AACTTGGAAT GGCTCCCGTT GCCTAGAGGA 180
TGGGTGCAAA CTCCTTGGTA TGACACACAA AGCCCTCTGT ATTCTGGCTA CTGTGGTTTG 240
TCTCAGCAGT CCTCCCTCCA ACTGCATTCT TGCGACATGC TAAGTTTCCA GTTCCAGCTG 300
TCACGCTGCT CCTTTCCCCA CATCTCCCAT ACCTTTGTTT GTACTGCTCC TTCTGCCAGG 360
AATGCCTTCT GCCAAGAATG CCACCTACAA CAGCTGTTTA CTTCTCACTA CTATGCAAGG 420
AGGGCCCTGG CCTTCCACAC CATGAGCCTC CTTCCAGGGG CATCCACTGG GCTCTGCACG 480
TACTCCTGCC ACAGCTCCTG TAATATTTTG CTGTGTTGAC TTTTCATGCC TGAATCCAGC 540
TGCTCACAAT GAGCACATAG AGCAAAATGA ACTGTGTTTT ATAGTCCTTT GCCTTTCAGA 600
TGCCTAGATA GTGCTGACAA TGGAGGAAGC TAATGAAAAC TATCTTGCCC AATGACTGAT 660
GAATGGATGA ATCCAAAGCA GAAAACCAGT CTATTCTAGT CACCAACTAG AAGAGTTTGT 720
TTCATAGATT ATGTATGTCA GTGTTTAAAA TGCCACCAAC AAACTCTGTT TATTTTGTGA 780
GACCTGAATG 790
|
