| Tag | Content |
|---|
EnhancerAtlas ID | HS048-07687 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr11:116589260-116591010 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:116590342-116590360 | GGATGGATGGAAGGATGG | + | 6.6 | | NOTO | MA0710.1 | chr11:116589809-116589819 | GCTAATTAGC | + | 6.02 | | NOTO | MA0710.1 | chr11:116589809-116589819 | GCTAATTAGC | - | 6.02 | | ZNF263 | MA0528.1 | chr11:116590924-116590945 | TCCCTTCTTTCCTCCACCTCC | - | 6.2 | | ZNF263 | MA0528.1 | chr11:116590921-116590942 | TCTTCCCTTCTTTCCTCCACC | - | 6.93 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I116719 | chr11 | 116589781 | 116589930 |
|
Enhancer Sequence | GTGGCGAGAA AAGACCCATG CCCAACATGC ATGATGCAAA AGAGAGCGGG ATACATGCAT 60
AAGCAAGGCA TGAACCAAGC GCTGTGGGCA TTTAGGGAAA GAAGGTATTG CTTCCAGCTA 120
GTGGATAGGG CAGATTTGGT GGAGGAGGCT TCTTCTCTGG TCTGGAAGGA CAGGTGAAAT 180
GTGGTGATGA AGAAGGTAGG GCATTCCACA GAGGCAACAG CCCACACTGA GATCTGGAGA 240
TGAGAATACT AAGAAGGCGG GGAGAGTACC TCCCCTGAAT CTGGAGAAGG AAGGCAGCAG 300
TTGGAAGGGT CCTCTCTTCT GGGCCATCCG CTTCCTCCTC CACTACCATA TAGCTCTACC 360
CTCTCCACTG TGTGTTCATG GGTGATGTTA GGTGGGCACA GCCAAGGGAT GGCATGGAAG 420
AGGGGTTATC TCAGGGCCTG TCCTAGAGAA GCTTGGGCCT AGGACACCCT CAACAGGACC 480
ATACATGTAC CACCCCCGTT CTGCCACCTC CCTTTATCTG CCTCTCCAGC TTGGCCAAGG 540
TTCAGTGGTG CTAATTAGCA GCAGTTAGCT CAGCTCCCCC ATCCGGCCCC TCCGCCAGGG 600
CAGGGACGTG ACTGATCACT GAGGTTTCCT TTCTCTCCTG CAGGGAAGAC ACAGCAGGAA 660
GCTAGAGGCA GGGGGCAAGA GGAAGGAGAA GCAGCTCCAG GAGTTAGCTG AGGTGGATAA 720
TAGAGAGGGA ATGGACTTTG TTTGGACTAA ACATTGTCAT AGGCTTAAAG AGCTGAAGGC 780
TTCTCTAGCT CCTGCTTGGG CAGGACTTCT GATAATAAGA ACTCCTAGCA AGAAAGTGCT 840
TGTAAAACCC CTCTCCTACA CTGTCTCATT AGTTTAGTCC CCAAACAGCC ATAGAAGACA 900
GGCATTATCA TTATATTATC ATTATTATTG TTATTATTAC TTAATGTCTT TCTTCCTTGG 960
TCAATCTAAG ATCCACAAGG GGCAGGGATC ATGTCAACCT TGTCACGCTG TGTATCCTCA 1020
GTGCCACATA CCGTGCCCAG CATAGAGGTG ACATTCAATA AATAGTTGCT GGGTGGGTGG 1080
GTGGATGGAT GGAAGGATGG ATAGATGGAA TAATGGATGG ACAGAAAGGC AGGTGGATGA 1140
AGGATAAATT ATCCCATTTT ACAAATTAAG AAACTAAGGA CCAGAGAGAA AAAGTGACTT 1200
ACCCAAGACT AATCAGACAG CGAGTGACAG AGCAGCACCC AGTCCCAGTT CACAGCCTCC 1260
CCATCGGGCC TGCTCGCAAT ACTCAAACTG TCTCTCTTCT TTGATTTCTT GAACACAATC 1320
CACCAAGAAA GGTCCACCCT TCTGAAGATC TGATTCTCAT CCTTCTTCCA GCAGCTGGTC 1380
AGAAGCCAAG CTCCTGCCAA CTCGGCTCCC ATAAAAAGAG CAGGATCCCG AGAGCCTAGT 1440
GACCAGGGAC TAGAGACACA GAGGCCCTTT CTGATCACTG GTCTGGAAGA ATCTGGCTGC 1500
CAACTGGTGA GGTAAAGGTA GACAGCGACA GCCAGAGTGC AAGTGCCCAT GGAAGAGCTG 1560
GCACCGACGG CCCTGTGTGA GCAGCACAGC ACTAGGAATC ACACAGATGC CAGTTCAAAG 1620
CCCCAGCACT TGCCCTTCCA CAAGCACCTG CCTCTGCAAC GTCTTCCCTT CTTTCCTCCA 1680
CCTCCATGCC CCTCACTCCC AACTTCTCCA AGCCCAGTCT CCTTATTGAT AGCATGGAGT 1740
CATGACGGCT 1750
|
