| Tag | Content |
|---|
EnhancerAtlas ID | HS050-12836 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:69980410-69982510 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr11:69982306-69982321 | AGGGCTGGCTGACCC | - | 6.02 | | ZNF263 | MA0528.1 | chr11:69982116-69982137 | CCCCCCAGACCTCCCTCCTTC | - | 6.42 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_01662 | chr11:69977616-69983019 | Aorta |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I070136 | chr11 | 69981721 | 69981870 | | GH11I070135 | chr11 | 69981923 | 69982368 |
|
Enhancer Sequence | TGACCCCTGT AGCACTGAGC CCCCTGAGCC ACTAGAAGAT TGTTCAGTGC CGCCTGCTGT 60
GGTCAGCCCT GCTGCCCCGT GTACATTTCT ATAGCGCCCC CGGGGCTCAG ACTCCCGCTC 120
TGCCAGTTCC CACCTCACTG CTCTAAACCT CAGCTTCCTC ATCTGCAGAA TGAGGCTGCA 180
TGAGGATCAG AGGCGACGGA CATGAACTCT CAGCCGAGGC TTAGCACATA GCTTACTCTA 240
AATAGGTGGT CACTGCCGTC TTACCACATT GGAGCATGTG AGAACCAAAG AAAACCTATA 300
CGAGAGTGTG CGTGCGCCTG GTGTGTGGGA GGTACTCATC AGCCACGTGT ACTGAGCACA 360
TGTGTCCCAC CTGCATGAGG ATGTGCACGT GCCTGGTGTG TGGGAGCTAC TCATCGGCCC 420
ATGTGTACTG AGCACAATGT GTATCCCACA CTGTGCCGGG CCCCAGGGGA ACCAAGGGAA 480
GCAAACCTGA TGTATCCGCT GCTCTAAAAG CTGCAGCGTA GGTTTCAAGA GAAGGCCCCA 540
TGGGAAGGGT GCGGGGCTGT GGCAGGAGCT CCAGGTGCAG GGACCAGGTG AGAGGGGTGT 600
CAGAGCATCC GGAGAGGTCA GCAAGGACAC GCTGAGAAGA ACTTAGTGTG CTGGCTCAGA 660
GGAATCAGAA CCCAGTGCCA TCAGCTGCTG TGTCAAAGAT GCTTTCCTGT CTTATGCTCG 720
AGTCGGAGAC CGCAAGTCTA AGAGGGAGCT TGTGCAGTGA TTAAGAGAGG GGTGACACAG 780
TGGGGGCCCA GCTCCAGGAA GGGCACCTAT GGGAAGGTGT GAGAGAAGCG ATTGGGAGCC 840
TCATGGCACC CTCCCTCCCT GGCCCTGGGG ACCCTGATTT CATCCGTCTG TTTCCTCTTT 900
CCCTGCTGAA ATCCCTGGGA GGAATTCAGC CCTTAGACTC CCTGTAGCCA CTTCTCCAAA 960
GAAAAGGCCT CCGATGGAAA AGAGAGACTT TAGATTATTC CAAAGGACTC CACACTTTGT 1020
TTTAGCTCTC ATGCTATTCC CATGAGTTAA GGAGACGCTG GCGGGCTTGG CCGAGCTGGT 1080
CTCATCTGAC ACACAGGGTT ATGAATTACA GCTCCCACAT TTAACCATGA ATAAAAGGCT 1140
TTTAAGGGCC CTGGAGAAAG CAGCCACCAC GTCCTTCCAC CCCACGCTCT GCCCATCCCT 1200
GGCATCACCT TAGGATCTGG GAGGGCACAG CCGTCTGAGA ACCCCTGGCT GGTGTTCTTC 1260
TCTACAGCGG ACTCCAAAGG CACCCACTTT TGTGGGACTC TCCAAACGTC CAGTAATTCC 1320
TGGGTCCACA GAACTGGGCC TCCCTCCTCT GCAGAGAAAG AAGGACGTGG TGTTTCATTT 1380
TCTCCTTCTC CAATTACAGG CATGCCCAGT AAGAGCACAT TCCCAGGGGA AGGGAGGAGA 1440
GAGGCTGAAG GAGCCCGGAT GAAGAAAGAA GCCGTCTTGG GCTGTAATGA TCCCATTTCG 1500
AGCTTAACAC GCCGGGCGAT AAGAGGTCTC TGTGATAAGC GCCTGTTGCG GCTCTTGTTT 1560
TGGGAGCCCA AAGCGCTACG TGGCATTCTG GTCACTGCAA ATTCCTTCTT CTGAGTGCCA 1620
GAGCATCACC CAGTCACGCC TTCCAGGTCA CCTGTGGGAG TGCCTACTGG GCAGGCATGG 1680
GTGCCGCAGC CACAGAACGA GCCCCTCCCC CCAGACCTCC CTCCTTCTGG GAGTTCCTGC 1740
TGCAAGGTCG TCCTTTGAGA GGATGCAGGC AGCGCAGATT GGTCAACACC CTGGTTGTTT 1800
GGGGAGAAAC CCTCAAGGGT CTGGTCCCTC ATGCGTTGGG CTGGCTAGCA GCCCTGTGGC 1860
CCCCAGGCCT GTGGACCCTC CAAGACTAGA GCGTCCAGGG CTGGCTGACC CTGCTGGAGG 1920
CTCTAGACCT GGGCCTGATT CCCAGGGGGC AGCAGCTCTG GGCTTGTCGG TCCCCTGTGG 1980
TTCTCAAACT CGGTCCCACA GGCCTCTGCA GGAACCCGCA CCAGTCAAGA GGTTTAAGTG 2040
CAAGGGAGGG ATGCCTGGGT ACAGCATGGA TGTTGGCATC TCGTCTTAGG TGCCCATGAC 2100
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