Tag | Content |
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EnhancerAtlas ID | HS182-17433 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:16913320-16914740 |
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) |
Klf1 | MA0493.1 | chr5:16913788-16913799 | TGGGTGTGGCT | - | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_32071 | chr5:16913468-16915251 | Gastric | SE_37080 | chr5:16912904-16915428 | HSMMtube | SE_47263 | chr5:16912081-16918919 | Panc1 | SE_63946 | chr5:16913308-16914474 | HSMM |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I016912 | chr5 | 16912273 | 16915413 |
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Enhancer Sequence | ACTCAAAGAC AAAGATACAA GCCACTGCCA AAATTCTCTT AACACTCCTG TCAGGTCATT 60 TTAAAAAATC AAATCTTGAG TAATAGTCAA GTCTCCTCTA GCAATAAAGC ACAGAGATGC 120 ATAGTTGGTA ATGCTAGAAG GAATCCAAGC CTTTAGGGTA TGAATTGCAT ATGAACATTT 180 CAAACTACAA TCTTCTGCTT CTCCTTGTAT ATACGTGTAT GGCTGTCTAA AGCTCAAGAC 240 TGAATGATTA ATTTTGGTTT TCACCCTGGT ATCGCAGAAT TTCCTTCTTC TCAAGTTTGT 300 GAATGAAGTC ACTTTTGCAA AACTGCATCT GCCACTGTGG AGGTGGCCAG TGCCCAGAGT 360 GCCAGGGAAG GCTGGCAGTG GAAGACAGGC TACTGACCTG CCTGCTTACA GAAACACAGC 420 CAACCCCAGG CAGTGGACAA AGCAAGCGTA GGTGTGCAAT GTGGGGTTTG GGTGTGGCTA 480 GGAGCCTGCA ACATCTTGAG TCAGAACAAG AGAGACAAGT GAGAACCAGG ATACGTAAGT 540 ATGAGCTGAA GTTCAGAAAT AAGGCCAGCA AAATTCTGAG CTCCAAGAAC AACAGGCCAG 600 GCAAAGACTA GACCACCATG TGGCAAGAGA GGGAGGAGGT TAGGATACAG TTGCTCGAGA 660 CAAAAAGACA AGAAGGAGAG GGAGCCAAGA GGCACCAGGA GGAGGAATGA CCTGGATCAC 720 GTGGGATACT ACACTCAGCC CCTTTTATGG GATTTCAGTT AAGACAAGAA ACAATACAAC 780 ACAGCTAACC TGGGCTCCTC CCTGGAAACA CACCTGAAGA TACCAACTTC AGTGGTGGGG 840 CAGGAAAAGC AAAGGAACAT GAGCAAGTCT GTCCGATCCT GACCAAATGA TAAAGACCTT 900 AATGTTCCAG CATGGTACTG CAAGCTGGGC CAAGGGTTCA AGGTGGCATT TCTTCCTACA 960 GTACCTACGG GAAGCTGGGT AGAGACCAGG GTGTTTTATA GGAAGTGCGG GCGGCTTGGC 1020 TGAGTGCCCA CTGCCAGAGC CAGCTCTGCC GATCCCAACA GCTGGCCATG CCGCCTTCCT 1080 TCGCTGCCAT TCCACATGAT TCCTGCCTGT GACAAACTTC CCAAGGACCT TCAGGAGCTT 1140 CTGCTGGAAT ACACTAAGAA GCCTGCAAGC CCATTCTTAT AAGAACCTAA CATGCGTTAT 1200 CAGTATCAGA TAGCGGTCAG CAGAACAGAT CAATATGCCC CATGACCTCA CTGGGATCAG 1260 TGATATCTGA CAGAACCTAC GTGGCCCACC TATGCCACTG TTAATTCTGC AGACCTGTTC 1320 TTTCTGCTGA GTCTACTACT TTTGTTTTGC CTATTTGTAA ATACTAATTT TTCTAGCCCC 1380 AGATATGTCT TTCCTACATT TAAGGGAGTC CTAGACAAAA 1420
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