Tag | Content |
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EnhancerAtlas ID | HS182-14802 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr22:24485360-24487530 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:24486928-24486946 | TTTTCCTTCCTTCCTAGC | - | 6.19 | EWSR1-FLI1 | MA0149.1 | chr22:24486924-24486942 | CCTCTTTTCCTTCCTTCC | - | 6.52 | EWSR1-FLI1 | MA0149.1 | chr22:24485473-24485491 | GGAGGGAGGGAAGGTAGG | + | 7.37 | Stat6 | MA0520.1 | chr22:24486487-24486502 | TTTTTCCTGAGAAGT | + | 6.83 | ZNF263 | MA0528.1 | chr22:24485474-24485495 | GAGGGAGGGAAGGTAGGGGGA | + | 6.34 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I024091 | chr22 | 24487437 | 24489361 |
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Enhancer Sequence | CCATTGGCCC AGGAAGCTCA GGTCCTGAAA CTGGGTTCCC AAGCCATCTT GTTGGAGTGT 60 TAGGGTGGCA GGAGAGAGAT GGAAATCCAC CAGGAATGCA GATGTCCCGA CAGGGAGGGA 120 GGGAAGGTAG GGGGAGGTGT TTCATAGTTG CCGAGGGTGA AAACTACCTT GCAGAGCTGC 180 CTTGTGCCTC CTGGGTTTTT TCCACCTCTG GAGAGACAGC TTCCAACCCT GAAATGTGTC 240 ACGAGGACAC AGTCCCCTGA TTGCTACTTT TCTGTCTGGA TTTATTGTGT CTGGAGGATG 300 GGCTGCAGGA CACATGTTGG CAGCTGTTCG AGCTGCTGTG TGCTTCAGCT TTTGCCCAGA 360 AACTCCTCAG AGGTGGTGGT GTAGGAGAAC AAATGCTTTC CCCATGATGT CAGTTCTCAG 420 GCAAGGGGAA AGGCTTTGGA GCCAGAGCGT TCTAGCTGTA TGACCTGGAA GCAGTAACCT 480 GACATTCCTG TTGTGGTTCC TTCTCCAAGG CAGTATTGTG AGAGTTCATT GGGAACACCT 540 GCCATCAGCC ATTTCCTGAG CCCCTCTCAT GGGCACCCCA TATGCAAGGT GAATGAGGTG 600 CCTATTCTGC TCTGAGGATG GCAAGGTAGT GAGATGGTGT CTAGTAGAGC TTCTGAAACA 660 CAGCAGGCCC TCAGTGACTG TCCCTCCTTT TCCTGTCTGA GGTATTGTGA CCTCCACACC 720 ACAAGGACAG GGACATTGGC ATTGTGCCCT GTATGGGGAA GGGGTGGGGG CTTAGCCTCT 780 TCCCAAGGGT CTGCATGGTA CCAGATGCCA GCCCAGATGG GCCACTTCAC AGCTACCCTT 840 TCTTTCTTGG CAGGTGGCTG TTACAGGTGC CAGTGGCAGA ACAGGGTGGG CAGGGGGGCT 900 AGTGACTTGG TCCAGGTCAC ACAGCTACAA AGCAATTCAA GTAGAAGGAC ATCCTTTTAG 960 CCATTGCCTT TTACTTCAGC ACATTTGCCA CAGAATCCCA TCTTGAAGGG GATGTGATGG 1020 AGTCACTTGG TTGGTCCCGT GTTTGACCCT GCACTGTGAT GCTTTCCACT GTATTTCACC 1080 CATTGATGAT CTCCCACTTC CTGTGTGGTC ATTTTTTTTT TTTTTTTTTT TTCCTGAGAA 1140 GTGTCTAACA GAGCACTGGG TAGCACATTG CTCCCTTATT TCAGTCCTGG GGCCATTGCT 1200 ACAGGGTTTT CACATAAACA AGCACCCACT GGAGAGACAT CCAAGGGCCG GCTCAACCTG 1260 GCTGGATGAG AACATGAGGC ACTTCCTGCA GGCCACAGCA GCTGCCCTTG CCAGAGACTA 1320 GTGCCTGCAG ACTCATCCCC TCTCACTGGC CCCTGAGGTC AGGCAAGAAG AGACTTTGGC 1380 TTCCCTGCTA TCAATCCAGG ACCACAGAGA GGAGGGATCA GAGACCTGGG CTGCTCAGAG 1440 CAGCTCTGTG GGCTTGCACA TGCAGGCTTC TCTCTAGCTT CCAGCCCAGA GTTCTGGAAT 1500 CAGGGGTCAT GAATTTGGCT GGCAGCTGAC CAGTATTGGA AAGTAGTGCC TCTTAAAAGG 1560 TGACCCTCTT TTCCTTCCTT CCTAGCTAGC TGTTTCCTTC CTTCAGGCTG TGAGAGGGTG 1620 GCTGGAGGTG CTTGCTGCAA ATGCAGACTC CCAGTCAGTG GCTCTTAAGT GGGGCTCAGG 1680 AATTTGCCCT TCTACAAGTA CTCCACATCT GTCTTAAAGA GCACAGAGGA GATGGTGGGA 1740 AGTCCTCTTG TACCCCAGGG GTACACACCC TCTCCTGTGC AGTGGAACTG GGTGCTAAAT 1800 ACATGCCCTC TTCAGTGCCG TAGGGCTGGG TGCTGAGTGT TAGTAAATGT CCTCTCCAGT 1860 GCTGTGGAGC AGGGTGCTAG GTGAATCTGC ATTAGATGCT GCAGGGGGAA AGCAGAAAAA 1920 AGTACCCTGG TTGACATGGG GTGACCTGAG TTTAAGTCCT GCTCTATGCC TTGCTTGGTG 1980 GGCGCTTTTG AGAAACCCCT AGGCCTTTCT ACACTTCGGT GTCACCAGCT GTGAAATGGT 2040 GAGGGCATTT CTGTGTCTTG GTTGTTAAGA GGAGTATAAA CTTGCAAATA GGTCGGCAGA 2100 GCTTTGTACA GGAAAAAGTC TGATCCCTGG GCAGGTTCAG GCGTAAGGCC AGCCCAGTCT 2160 CATGATCTTC 2170
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