| Tag | Content |
|---|
EnhancerAtlas ID | HS092-16965 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:101473450-101476150 |
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 | chr14:101475941-101475959 | TCCTCCTCGCTTCCTTCC | - | 6.42 | | EWSR1-FLI1 | MA0149.1 | chr14:101474569-101474587 | CCCTCCTTCCCTGCTTCC | - | 7.14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I101008 | chr14 | 101474961 | 101475110 |
|
Enhancer Sequence | CAGCAACAGC TGGTGACCCC GGCCGGCCCC CTGCCAGCCG GGGCTGCTGG CGGCCGCCCA 60
GAGGGGAGAA AGGCCCTCCT GGGCACACAC GGTCCTGCTG CGGGCTCCCT TGCCTCAGCT 120
GCCCACCCCC CAACCCATTG CTGCTGGGCT CCTGGCTTCA TTTATTGATG GACTCTCCTG 180
TGGGGTTCTC CGGGGAACCC CAAGCCAGAG TTCAGACTTC ATAAGGGGCT GCTTAACTGA 240
CACCCTCTGT CACAGGGTTC CCCTGTCCTC CTCTGCGACC CTGGCCCCTG GCCCACTCAT 300
TTGCGCGCAG CTGTGCTCTA CATTCCCACC CCCTGCTCCC TGCAAAACCC CACTGCCCTG 360
CAGGCTACAA ATCCAAAGAT TGGGTGCTCA TCAGAGTTGG AGAAGCCATA TTGGAGGGGA 420
GGGGTCCCAA AGGTAGCAGC AACCCCTTTA AAGCCATGGA GTTGGGTGCC AAGGGCCACC 480
CGGGGCCCTC TGGTCCCCTG CTGCTGCATT AAAGGTCTCC TGGCTTCTTC TCCTTCCAGG 540
CTTCCTCCTT GCCATCCTTT CTCGGGGACT GTGGCTTGGT CATGATGTGT GGCCTGGGTT 600
TGGATTTGTA TTGTGAGGAA GAGGAGACAG AGTGGGGTGT GTCACAAAGG CTGAGATGAG 660
CAGGAAATCA AGCCTTGCTA GTTGGTTTTC TGGAGTGGAA TTGAGCCTTA AGAAATGAGA 720
TTTGTGAGGG CCAGGTGTGG TGGCTCATGC CTGTAATCCC GGTGCTTTGG GAGACCAGGT 780
GGGAGGCTAG CTTGAGGCCG AGAGACCAGC CTGGGTAACA TAGCAAGACC CAGTCTCTAC 840
AAAAAATAAA AAGATGAGCT GGGTGTGTTG GTGCATGCCT GCGGTCCCAG CTACTCAGGA 900
GTCTGAGGTG GGAGGATCTC TGGGGTCCTT GGGATGCCCC CCTACCCCCA CATCTAGCGT 960
GGCTTTGTGC CACTGCACTC CAGCCTGGGT GATAGAGCAA GGTCCTATCT CTAAGAAAAG 1020
AAGAAAGAAA AAAAAATGAG GCATGTGAGC TGGAAACAAG GGAAGCAGAG GTGCTTCATG 1080
TTCCCCAGCG CAACCCCGCA TGACCCCCCA GGGAGCTGTC CCTCCTTCCC TGCTTCCCTG 1140
ACATGGGTGG CGTCTGTGCT GCCACACTGG CCACTTTGCT GAAGCCTGCC AGTGTTGCCG 1200
GCGGAGGGGG GGTTGCGGTG CCACTTGCCT TCTTTACAGA GAAGGAAACT GAGGCTCAGA 1260
TGAGTGCAGA CAGCCCAAGC CTGTATCAAG TCTGGGGCGC ATCTCACATC CCCACACCTG 1320
CCTCCAGTAC TGCTCACCGC ACCCGGGACA CACAGGTAGG GGTTTGAAGC AGAAGCTGGC 1380
AGCGGCTCTG TCTGCAGAGG CTGGTTGCCT TGTCTCGCAC CTGTGGGCTT GGGTCAGGGC 1440
CTCTTTCACG TGAAGGTTTC CATCCCGAGA GCACTGCAGC ACATGTTCAT GGTTTGCTCA 1500
TCAGGACGAA AGAACTTACA AAACTTTCCT GTCCAAGTTG ACCAACTTGG TGATTTTTCA 1560
TAAAGCCCCG CAGCAAGGCA TCTGGAAAGC TCCTTTCCTG CTCCTGACAG TCACCCCGAA 1620
CGGCATGTTT CCAAATCCAC AGAACATATG GGCTGCAGAG CTCAGAGCCT TGCTCCTGGC 1680
CCAGCCAACA GGATGCTCTC TTCTTTCCCT GGCGTGGGTA CAGGGGCCAC TCTCAGCTGC 1740
CTGGGCTTGC CCCCAGCCCT AGAGCCTTGC CTTTGGTACC CACTCGCTTG CCTCCAAATT 1800
CCTGCGTCCA TGACCTCAGG GACAGCCCCC CTTGGTGCTC ATCTGTTATG AATACCAGCC 1860
CATTTTTTTC CCAGCAAGGA AAGCCTGGCT GAGTCAGTTC CTGGGCCAAG ATTGGCATGG 1920
AAGGAACTCT ACTGATAGGA GCAGGCAGTG AGCATGCAAA GCACAGCTCC TAAACCCAGG 1980
GTCAGGTCAT AGCCAGTGGC TGTCAGAGCC TCAGATGGAA GAGCCAGCGG GAAGCCCCCG 2040
GCCCACCTGG CTGTATGGGA CATTGACCCG GCACAGGGAG AAGACCCAGG GGGATGTAAG 2100
TTAGTTACTC TTCTAGCTCT GGGTTGGAGG CTGGGCTTAT GCATGGGCAC TGAATCCTTA 2160
AAAAGTTAAA TGAAGATACT AAAATAGAGC CACTCATGGA CTCATGTTGA TTGGTGTCAG 2220
AATAAAGACT ATAATCAGTC CAATTCTGTG TATATTTCAG TTTGAGGACA ATGATAGTAA 2280
TAACAAAATA TAGCAATAAC TTGACTGGTC TAAACCTCAG TGCATTGCTC TACTTGGCCA 2340
AACCTATATA CCCCCCTTCC CCCATGTTCC TTTATCTCAA TGAATGGCCT CAGTAATCCT 2400
GAAACCAAGG TCGGCTGCAT CTTCTTCCTC CCTGCACCCT CCAGGAGCAA TCCATCAGTA 2460
AGTCCTATCA GCGTGACACC GTGAATGCCT CTCCTCCTCG CTTCCTTCCA GTTGCCCCTG 2520
CCTGGTCACA GGCCTCATCC TCCCTCTCTG GCCCAATTGG ATGCCCTCTG CTTGCTTGCC 2580
TCGTCTCTGA CTGTATCCTG TGGGTGACAT GCATGCATAC CCGGTACCAC TTAAACCCCC 2640
CATGGGCTCC AGGGGCCCCA CTTGTGGTGT ACCAAGCCAC TCTATCCCCT TGGCCCTGTG 2700
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