Tag | Content |
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EnhancerAtlas ID | HS082-03248 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:224822100-224824010 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:224823400-224823418 | TTTTCCTCCCTTCCTTCG | - | 6.41 | Stat6 | MA0520.1 | chr1:224822439-224822454 | CTCTTCCTAAGAAAT | + | 6.35 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_56486 | chr1:224822267-224824534 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I224634 | chr1 | 224822366 | 224823919 |
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Enhancer Sequence | TCTCTACTAA AAGTACAAAA ATTAGCTGGG CATGGTGGCA CGCGCCTGTA GTCCCAGCTA 60 CTCAGGAGGC TGAGGCAGGA GAATTGCTTG AAACTGGGAG GTGGATGGAG GTTGCAGTGA 120 GCCGAGATTG TGCCACGGCA CTCCAGCCTG GGCAACAGAT TGAGACTCTG TCTCCAAAAA 180 AAAAAATAAA AAAAAAAAGG TTTTTTGCTA GCTTGGTGTC TCCCAGTCAG TGCAGGCCCA 240 AATTCTAGAG GATAAATGGT AAAGTGAAAC CTAGCTCTTC CTTTCCTTTT CTTCTTACTG 300 TCCCCCATGG AGCATAAGCC CTTGCCTCGC AACTCACTCC TCTTCCTAAG AAATGCCCCC 360 CTGCCCAGTT ACCCTGCATC TGTTCTGTGT TGAGCAGAGG TGTTCAATTT CACGTCCCCG 420 ATTCACACCA AGCCTCGGCC CTACCTGCAC CACTTAATAT GCCCCGCTGC ATCCCCGCCA 480 GGAGCTGCTA GCTCATAATT AGCAAAGTTG GCAGTTTTCA GCACTGTTCA GAGTATAAGT 540 TGTTTTGCTC CATAAATGGG AGGCAGCATC CGTTGTCTCA CAAGGGGTGT GTTAGTTCAT 600 TTTCACACTG CTATAAAGAA CTACCTGAGA CTGGGTAATT TATAAAGAAC AGGTTTAATT 660 GACTCACAGT TCTGCATGGC TGGAGAGGCC TCAGGAAACT TATAATCATG GCAGAAGGTA 720 AGGGGAAGCA AGGGACATCT TACATGGTGG TAGGACAGAG AATGGCGGGG GTCGGGGGGA 780 ACTGCCCTAA ACACTTTTAA ACCATCAGAT CTTGTGAGAT CTCACTCACT ATCATGAGAA 840 CAGCATGGGG GAATCTGCAC CCATGATCCA ATCACCTCCC ACCAGGCCCC TCCCACGACA 900 CTTGGGGATT ACTATTCGAG ATGAGATTTG GGTGGGGACA CACAGCCAAA CCCTACCAAG 960 GGGAGAGGTG ATATTATGGC TCAAAGCTAT GCTGTGTGCT GGCACCTCTG TTAAAATGAG 1020 TTTCTTAAAG AAGCCAAATA AAGTTTGGTG TGGCAAGATT ATTAAAATCA ACAGAGAAAT 1080 GACTGTAGGA ACAGCAAGCA TTTTCAAGAA GTGAGTCCTG CTGAGCAACA GGGAGGAAAA 1140 TAAAGTGCCG GGGGCTGTGC TAGGACAGGG ATGCTGACTC AGACCTCACA GCACAGCCGA 1200 GCCGGCCTCG GCCTTGGACA TGAGCAGTCA GCCCACAGCA TGCAAAAGTT TGGTTGTTTC 1260 TGAGACCTAC TTCTTAGCTT AGTCCATATA TTTCTTCACT TTTTCCTCCC TTCCTTCGTT 1320 AGAGACAGGG TCTCACTTTG TTGCCTGGGC TAGAGAGCAG TGGTGTAATC ATAGCTCACT 1380 CTCACCTTGA ACTCCTGGGC TCAACTGGGC TCAAGCATTC CTCCTGCCTC AGCTTTCTGA 1440 GTAGCTGGGA TTACAGGTGT GTGCCACCAC ACCTGGCTCA TTTTTTTTTC TTTCTAGAAA 1500 TGGGGGGGTC TCACTCCGTT GCCCACGTTG ATCTTGAACT CCTGGCTTCA AGTGATCCTC 1560 CTGCCTTGGC CTCCCAAAGC ACTGGGATTA CTGCGTGAAC CCTCTTTTTT ATATCAAAAT 1620 ACCAAGTGGA ATGTTTCGTT TAAGAAAACA AAAATCAACA ATACAGCAAG CCAAAACCCA 1680 AGACAGTAAA ACGTCTGGGG TCAAGGGCTT AACCAGGAGC AGCTGTGGCA CCCCGTTGTT 1740 AGAAGTGTTG GTTGCTCTGT GTTGGTGCAC CAGGTCTTAG CTGATGGCAC CATCCTTCTG 1800 GTAATGGGGT TGGGTTGGGT GAGTTCGGTT TACCATTTGC ATATTTGTTT TCTTTTAATT 1860 TGACTACATT GATGAAAGAG GGATACAGTC ATGTAATCAC ATAGTCCTGG 1910
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