| Tag | Content |
|---|
EnhancerAtlas ID | HS103-07211 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr13:109510730-109513170 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr13:109511323-109511341 | CATTCCTCCCTCCCTTCA | - | 6.22 | | Foxa2 | MA0047.2 | chr13:109512169-109512181 | ACAAAGTAAACA | - | 6.18 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I108858 | chr13 | 109510913 | 109512608 |
|
Enhancer Sequence | AAATACCCGA ATTTGGTCAT TTGAGCTCTT CCAACCTGCA CGTCTCATGG CCTTTCCTCC 60
CTGGCTCATG GCAGCCCCAC TCTTGTCACT TCTTGGGCCA ATGCATTTGG TGAGACTGTT 120
GATGCTGGTT TTCCTTCCAC ACCCCACATC TGATTTCCCT GCAAATGTCA CCGGCCCTAC 180
CTTCAAGTTA TACACAGAAG GCCACCCCCA CTGCTGCCTC CAGGTACATA TCTTCCTACA 240
GCAATTGCAT TTTGCACTTG CATTTTATCC TGCAAATAAG TGTCTGGGCT TCTCTTGACC 300
TCCCCTCTGT CTATTCTCAA CACAAAAATT CAGAGTAACA GTGTTAGAAT GCACATTGCA 360
TTATGACACT TCTCTGCTAA AAAGATGCCC AATTCACTCA GTAAAGCCAG AGTCTGAGGA 420
AAGGCTCATA AAGCCGCAAC GCTTTCCCCC TACCTTTTGA ATTTCTGACG TCAGATGCTG 480
GCACCCTACC CTGGGTGCCT CTACCCTGGC CACATTGCTG GCCTTGGTGT CTCATGAGTA 540
TGGGCAGCAC TTCGGTGCAG GGCTTTGCCT GAGTAATTTG ACCACCATAT GCCCATTCCT 600
CCCTCCCTTC AGGTCTTCAT ATCAATGTCA TTGCTTCTGG AGGCCAGCCC CCAGTCTATT 660
TGAAATCGCA AAATGCACTT CCTATCCTTC TGCCTTCATA TGTTTTCCTC CACAAACTTA 720
CCACTCTCTA ACATACTGTA TATTTTTCTT ATTTAGATTC TTATAAATAC CATGTGCTGA 780
TTCTCCCTAC AAACACAGAC TGTCTGTCTC TCTCTTTCTA TCATGCCCAT ACCCACTAGA 840
ATGCAAGTTC TATAAGGAAA ATAATTCTTG TTTTGTTCAC TGCTATGTAT GACCCATAAT 900
AGGTTCCCAA TAAATATTGA ATAAATAAGT AGACTTCCTC AACCAAAACC CTAATTTTAG 960
ACGAGAGAAA GAAGTTAATA TTTACTCATC CATACCAAAT AACTGAGGGT TGAGCAATGA 1020
TTTGTTTTCA GAGCCAAGAT AAAATATTTT AGCTGACTTA ATCATTTGAC CAGGATTTTC 1080
ATCTCTTTTT GCTACAGTCC GATTTTTTTT ATAGTATGAT CTTTCAAAAC AGATTGTAAA 1140
TTGCCTTTTT ACTAAGTATA TAACCTTCTA TTTGGACGTT AGATTAGGGA GTTTCCACAG 1200
TCTGCAGTAT TAGGGAGTTC TCCAACCTTC AAACAGAAAA TGAAATGCGT GTGATGAGAC 1260
ACATGCTCGC CAGGAAATGC ACAGAATACA AGCGTTGCAT TCTCTGAATA CTTACTGCCA 1320
GCAGCCCCAG AGAGAACAGA ATATGCAGTC AAATTCCTTT ATGGACAGCA AAGAAGTTTG 1380
CTGGAAGTAT TTATTTTACA AGCACATTAG TGGGACTTGA GACTCATAAA AAAAACCCCA 1440
CAAAGTAAAC ACAAGACCTC CTGTAACATC TGGTTAGCCA AGAGAATTCT GAAACAAATA 1500
TATTGTAATT GGATAAAAGC AAACCAGAGC AATAAAGCAT CGCATGACAG CTCCTAGTAC 1560
ACAGCCTCAC TCATTTCAGC CACTTAACAT GCCACTCCGG GTGACCCAGG TTAATGTAGC 1620
AGAGCCTCTT TTTTTTTTTA ACTTTTATTT TAGGTTTGGG TTGTAAAGGT TTGTTATACA 1680
GGTAAACACG TGTCATAGAG GTTTGTTGTA CAGATTATTT TATAACCCAG GTATTAAGTC 1740
CAGTACCCAA TAGTTATATT TTCTGCTCCT CTCCCCCATT CCAGCCTCCT TGGCCAAGTA 1800
GGCCCTGGTG ACTACCGTTT CCTTCTTTGC ATTCATAAGT TCCTATCATT TACCTCCCAT 1860
TTATAAGGAG AACATGAGTT TGGTTTTCTG TTCCTGTGTT AGTTTGCTAA GGATAATAGC 1920
CTCCAGCTCC ATCCATGTTT CCATAAAAGA CATGATCTTG TTCTTTTTTA TGGCTGCATA 1980
GTCCTCTATG ATGCACATGT ACCATTCTTT CTTTATCCAA TCTGTCATTT ATGGGCATTG 2040
AAATTGATTC TATGTCTTTG CTATTGTGAA TAGTGCTGCC ATGAACATTC GTGTGCATGT 2100
ATGTTTATGG TAGAGTGATT TATAATTCTT TGGGTATATA CCCGGTAATG GGATTGCTGG 2160
GTTGAATAGT AATTCTGCTT TTAGCTCTTT GAGGTATCAC AGTACTGCTT TCCAGAATGT 2220
TTGAACTAAT TTACACTCCC AACAACAGTG TACTGCTGCA CATCTGTGAC CATCTGTTCT 2280
TGGACAGAGC TGATAAAAAC AAGCAATGAG GAAAAGATTC CCTCTTCAAT AAATGGTGCT 2340
GGGACAACCG GCTAACCATA AGCAGAAGAG TGAAGCTAGA CCCCTTCCTT GCCCCATATA 2400
CAAAAATTAA CTCAAGATGG ATTGAAGACA TAAATGTAAA 2440
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