Tag | Content |
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EnhancerAtlas ID | HS023-20329 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr5:87797590-87799260 |
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) |
IRF1 | MA0050.2 | chr5:87798369-87798390 | AAAAGAAAAGTGAAAGTTAAC | - | 7.77 | ZNF263 | MA0528.1 | chr5:87799047-87799068 | GGGGGAGGAGTGGCAAGAAAG | + | 6.3 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_63434 | chr5:87775638-87798996 | NCI-H69 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I088502 | chr5 | 87797923 | 87799216 |
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Enhancer Sequence | AATGCAACAA CAGAGGAGAG AAAACAGCTT GTCATAGAGA CCAGAGGCAC AGAGACTCTC 60 TGAGCAGCAA AGTGAGTCCT GAGGCAGTAA AGCCTCCCTG GTTGTCCCTG ACCATTTGGG 120 ACGAGGTCAC CACCCCAGGA TCCACAGATT GGGCCAGCAT AGAGATGTTT CTCCGAAAGA 180 CATGACAGCA GAGACTGATC ACCACATGCA TTGTATAAAC TTTGTAGATC ATTGTACCTG 240 ATTGTTCAGA GTCAATCATC TGTAGTTCTC ATTCCAGCCT TTAGTCATTC TCAAGAAATC 300 AAGAAAATGT CATTTTTGTA ATATTCTGAG TTCAAGAATC TCCCTACACA TGGGAAACAG 360 GTTACCCATA CCAATTAAAT CAGAATTTTG ATGCCCTGTG TGGACTAAAC CAGGGAAGCA 420 GCCTCTTCTA AATCCTGCTT CAATGAGGCT TATGTCTGCA TGGGTGTGCT ACTCATTGAA 480 CACAAATATA AAGGTGCCAC CAGACAAGGA GTTTTTCTGG TTCATCATTG CACTGCAGGA 540 TGCCATGAAG GAGTCACAGG CTGTGGCTTC CATGAAGCCC GTGACAAATT TAATACCCTA 600 TTACTTGTGT CGTCTGCACT AGCACTTCAT TTGGTGACAT CACTGGGTAC AACTAAAGTT 660 GAAATTTGTG TGACATTTTT GCAGGTGTTG CTTTTCACCA AAAATGTTAT TTTACATAGT 720 TTAGCCACAG TGCAGTGCTT TAAGTCTAGA ACTAAACCTC AGGAAATCTA ATGAGGTTGA 780 AAAGAAAAGT GAAAGTTAAC GGCTGCAGCT TTAACAAAGG CTCATCCTCC CTCCGGCTCT 840 AAAGAGTCAG TAACTGAGTT CAGTAACTGA AAATTAAATT AGAAGAAATG CCACCTCTGC 900 AGCTACAGCT ACCTTTAGCA TTAACAATAA TATAGAATGG GATGGGGGTG GGGGGTTCTG 960 CTCAATAGAG CCATCAAGAA ACTTTCAGAG CCTTTAAACG GGATGGAATC TGCTCTTACC 1020 ATGTTTTAAG CTTCCCTTGG TTTTATATTT TGCCCTCTCT CTAGCCTTCA TTTCCCTCAT 1080 AGCCATATCC TTGTCGTATT TTTTCTGTTC TCTCCTTTCT GCTGTTTTTT CCTCCATTGC 1140 AAGTCTTAAT TTCCATTTTC TTCTCTTCCC CCACTGCCAC ATTTTTTTCC TTGATTCTCT 1200 GAGTTTGTTT TCCCTCCCCT ACCATGTTTA CATCTTTACA AGAATAATTT AACTGATGAC 1260 AAGGTTTTTG TGATTTGCCC TGTTCAGAAT CTGGGAGAAA ACAGTTAAGG ATTCTCCAGG 1320 GCATAAGGCT TTTGACTTTA TCTGGTCACA TCAAATGAAC AGGAACCATT TTCTCAGGAT 1380 CGTATTATCA CAGTAAGTGA TAAGGATGTG CAGGAAGAAC TTACGAGCAG TGGCTCACAT 1440 TTAAAAAAAA AAGGCTGGGG GGAGGAGTGG CAAGAAAGGA AAACATATTA GCCTTTGTCA 1500 GGCTCCTCCC CATTCTTCAA ATAAGCATCT CTAAAAAACA ATCAAGCAAG GTTGTCAATT 1560 TGGCCAAAAA TCAGCAATGT TTTAATATAA TAAGATAGTA CTGCCACCCA TTTACTTCTA 1620 AACAAATTGT GAAAGAACCT AACTATATTA TATAGCTATA AAGAAATAAA 1670
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