| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06366 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:232245870-232246970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:232246613-232246628 | TGCCCTTTCACCTCT | - | 6.4 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33026 | chr1:232245888-232247267 | H1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I232109 | chr1 | 232245732 | 232247670 |
|
Enhancer Sequence | TCCCAAATCC AGCCCTCAGT TCTTTTCTAC TTCTCTTTGT CTCCCTTCTG TCGAGTCCTC 60
CAAATTTGTT TCCAGTCTTT CTTTTTTCTT CACTGTTTTA CTTGAGTCAG CTCAACTCCT 120
TTACAATCTC CATTCCCAAT TCTCAGGGCG CTTGTCGTGT TATCATGGAG TGCTGAAGAA 180
TGCATATAAA TAACACACTG GAATGTGGAG TAATTTTTCT ATCCACCCAG AGCCTCTAGA 240
AGCAGTAAAA AGAATTCCCC TTCAGCCATA TACATCTGGA CCCCACATGG GCTGGAGGAA 300
TGATGCTTAC TGTTCAAGTC TAGCCTCAAG AAATGCAACA TCAGAAATAG CTTGGCACCA 360
GGGCTGGGTA AGACTTGAAC AGCGCCTGAA CACCGCTGAC TTAGCTTGAG TAAGGGAACT 420
CACTGGGCCC TGCAGCTGTG ATCTCTCCCT GCAGACCTCA AGACCATTCC CTTTCCCCTC 480
CTAAGGGGAG AATGTCAATA CTCCTCTCCC TCGCCTGTAG CCGGTCCGCT CACAAGTGTG 540
CCTCTGCATA GTAGATCAGT GTGGCCCCCA CCCCCAATCT GCAGTCCTCA CTGACTCAGT 600
GGCCTGGCAT GGGGGCGGCA AACGCTGACC CTGAGCTGCT ACAGTTACCA GTAGCGGCTA 660
ATGTTGGTGA CAACCCTGGG GGGAGGGGAG CGGAATAAGG GGAATGGGAA GTGGGATTCT 720
GGGAGCCCTG TGGAGACTCT AGCTGCCCTT TCACCTCTCA GCTCTCTGAG CGATTTGTAT 780
TCCCAGTTCC CAGCTGTGAA TCCATGCAGT CGGCTGCAGA ATGCTAGGGA TAAAGTGCCA 840
AAAACCTAGC AGGAGGTGAG AAAGGAAAGC CTTTGTCATC ACCTCCACAC CGCTACCATG 900
CTGCGTCTGT GTTTATAAAA GGGGGAACAT AAACAGACTC GGGGAGACCT AATGATTTGG 960
GTTATGGGGC TTTGGAAGTG GCTGAAATTC TGCCCCTTGC TTTTTGTTGA CCCAGTAGAA 1020
GAAATATCAC CTAGGAGGAA CGCTTCAGAT AAGTCAGCTG TCAAGAAAGA GGTGAAGATG 1080
ATCAAATAAA TAAACTCAAC 1100
|
