| Tag | Content |
|---|
EnhancerAtlas ID | HS047-10722 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr14:96690800-96692630 |
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 | chr14:96691864-96691882 | GGAAGGAACGGATGAAAG | + | 6.06 | | SP1 | MA0079.4 | chr14:96692222-96692237 | GAGACCCCGCCCACC | + | 6.23 | | STAT1 | MA0137.3 | chr14:96692386-96692397 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr14:96692386-96692397 | TTTCTGGGAAA | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26721 | chr14:96690340-96692811 | Esophagus |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I096224 | chr14 | 96690401 | 96692851 |
|
Enhancer Sequence | AATATAAATG AAATGAAGAT ATGTTGCAGG CACTTTGCAC ATTGTCACGG TGCTCCCAGT 60
GCCTTGTTCC AGGGAGGTTA TCCTTATTTA CCAAGAGGTT AAGTCACCTG CCCTAGGTCT 120
TCCAGTCAGT GGAGGCAAAG CCAAGACATG TCCCGAGTTC ATCTGACTTC TGAGTTCAGG 180
CATGACCTGA ATGTTCTTGC CTCGGGCTCA GGGCTCAACA TTTCCTGTCT TCTCTGCTTC 240
TCCAGTCCTG AGAGATTCTG GGCCCGTTTC CCTGCAGATC AGCTCTAAGG AACATGCTTC 300
TCTCCTGCTC CTTTCTAGAA AAGGCGTAAC ATTGGCAGAA CCAGGAACTC TGGAATTCTG 360
AAGGTTGACT CCCTCAATTC CAAGGGGCTC CACCTCCTGA GCGGAATTGG ATAGAAGACA 420
AAGGTCACAT GGCTAGGGTG AGGCTTTGAG ATGGGCGAGA CTGTGAGCAG GACTGACAGG 480
TCAGGGCCAG GACCCAGGAT CTTCAGAAGC CACAGGGAGC AAGGCAGGGA GCAGCCTCCT 540
TTGTGCCACA CCCAGTGAAG GGGAACTTGC TAAGACAGAT TTGTTCCTCC CATCTCCAGA 600
AGAGCCGTTG GATGCCAATG GGTGAGGAGC TGAACCTCTG CAGACTCAGT GTGCTGATCC 660
CATTGCCTCT GCTTGCATGC CTCTCAGGAT GGGGAGTTCA CTGCATCCCC CTCTTTAAAG 720
ACATTACGGT TGTACAAAGG TCTCCAGAAT CATCTGTTAC ATCCCCTCAT TCTCCCAATG 780
AGGAAATTAA AGCTCAGAGA TGCCGAGGCA TTTACCCAAG GGCACACCTG GTCCTGGGCC 840
TACGACCCTT AGACAATATT CCTTCCACCT CTTTGCTATA GAGTCTCAGA CTAGGGATCT 900
TGGCTGGCTG AGAAATCAGG GAAGGCTTCT TAGAGGAGGT GAGATTGGAG GTGGCCCTTG 960
TAGGGTGGCA CTAAGATGTC GCTTGATATC CTAATTTTTT TTTTGGCCCT GCCCACCATG 1020
TGTGTGCCTG TGCTGCCATG TCACACTAAG CAGAGTAAAA TGAAGGAAGG AACGGATGAA 1080
AGGGGCAGGA AAGCGACTCC CAGGAGCTGA AAGGGCAATA GTATAGGTCC CTTCAGCACC 1140
TAGGATATGT TGTGGGAAGC CCTTAGACCC CAGATACTAC CCTGTGCAGA TAGGGATAAA 1200
ACTCCACCTG TCCCAGCTCA GTGCTCTCCC CGGCTCCTCT GGCCTGCTTG CTGGGCAGGG 1260
CCCAAACCAG TTCAGGATTC CTTTTTCTCT GTGACCTACC AGTTAGGGTT CTCTGTTTAC 1320
TGTGTCTCCT CCTCCTTGTT TTGTATACCC AGCTGGGTGG GAAGAAGGTC ACAGCCCAGG 1380
TTTGCACGTG GTGGAGGAGC AGGGCCAGTA ACTGGTTAGG CAGAGACCCC GCCCACCACC 1440
CTCCACTCCC ACCCTAGCAG GGCCTGTGCC ATCCCCAGGA CACCGGAGAC CACCAGGGGG 1500
CTGGAGAGGC TGCGGGAGAA ACAGCCTTCC TGGACACACC CAGCTACGGC TCACTTCCCA 1560
GCCTGAGCTG TTCCTTAGGA ATTGCTTTTC TGGGAAACAC ACCCTCTTCC AGACCTGCAG 1620
CCTTCCTTTC TATGTGGTTT TTGGTTTTGC TCTCTGGTGA GGGTTTCTAT TTTTTCCTGG 1680
TATACATGAA TGGCATGCAG GAAAGTGGAA TGAGGACATC ATGACCACCA TGCAAAGGCC 1740
ATTGCTCTTA AGGTTTGATG TAAGCTCCCC ACTCTCCACC CCCACTACCC CTCTGCCTCG 1800
GCCTGGGGTA TGAGGTCTTG GTTTTGACAA 1830
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