Tag | Content |
---|
EnhancerAtlas ID | HS182-10449 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr18:45579080-45581420 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr18:45579953-45579963 | ATCACCCCAT | - | 6.02 | ZNF263 | MA0528.1 | chr18:45580634-45580655 | GGAGCAGGGAGGGAAGGGCGG | + | 6.2 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26544 | chr18:45573812-45581208 | Esophagus |
|
| Number: 1 | ID | Chromosome | Start | End |
GH18I048054 | chr18 | 45581027 | 45581432 |
|
Enhancer Sequence | AAAATCCTAG CTCTGCTCTG CAACTGCTTC ATGTGACCTT GAAGCGGCCG GGTCCCTGTT 60 TGAGCTTCAG TTTCTTCTTT TATATAAGAC TAGCTGGTTG TGAATGTCCC TTGCTGCCCA 120 CACATGAATC CATTTCAATA TTTTGGTTCC AGGATAGATC CTTGGATTCT GAGGTCATGC 180 ACAGCTCGAC TTCAGATGTC TTGGGGCTGC TGCATCTCAC TTTGGGTTTC CTGTGACCTT 240 GACTTTGCCC TCTTTCTCCT CCCACCCCCT TCACTTTAGT TCTCTCTGGG ACCCTGCCAA 300 GTTACACAGG AAAATACATG TGAACACACG TTGGACTTTC AGATGACGAG TGTTCTACAA 360 GGTCAAGGTG GGGTTATTAT TTGACCACAG TGAGTAGAGT GATGACGACT CAACAGGTTG 420 GTAAAAGTGC TTGATGCGTC CCTTCCGCCT GCCCCAGAGG AAAAGTGAGG AGGCAGCTTC 480 CATGTCTGTC TTCCCATCGC CCCTACAGTG GCCAAGAATG GGCATGGAGT TGGGAGCGGC 540 CGCTTCTGCA GAATGTGCAC AGATTCATTA CAGACACCCC ACAGGCCTTG CATGCGCGGG 600 TTGGGGAATG GACAGGAACA CAACTCATTC TCCCATAATG GTGACTTCAG GTATGCTGCA 660 CAGAGACACA GTAAACAGGT GATGGAAGGA CCAATTCTGA GATTCCTTCA CCTTTGACTG 720 AATCAAACTG GTCACTGAGA TGTACTCTGG GTGCCCATTA GGTACCAGTC GCTGTCCTAA 780 ATATTTTACA TTTATATTTA TATTTATATT TGCATTTATA TTTCTCTCAT TTCATCCTCT 840 CAAAAACCCC ATGAGGTGGC TACTGTCATC ATTATCACCC CATTTTTCAA GTAGGGAAAC 900 TGAGGTAGAG CCGAGGCTTG AACCTAAGCA GTCAGGTTCC GGGTTTCCTA AGCAGTCTGC 960 AACTGTCTCT CTCAGCTACT GCAGTATTTA CCCATTTAGC TAAGTGCTGG AGAAACATGG 1020 ATGAAAGAGA TGGAGCTCCT GGTCTTAAGA AGCCACAGAA GAGTGGGAGA GACAGTAAAG 1080 ACAAGACCTA AAATGAGTGC TAAGTGCTGG TTCATGGAGG CAGATGGGGT GCCTGGGGTC 1140 AGAGGACGGG GACTCTGCTG GGCCCAGGAA GGGGACTCCT CCAAGGAGGT GAGGCCCCCA 1200 AGCAGCCAGG GATGTGGGGC AGGGGAAGGA CAACATTTTG GCAAAGGGAT TAGCTTGTGC 1260 GAAGGCATGC GCAGAGGCTG AGTGAGGATG GCACATGCAG ACAGGAATGC CAGGGAGTTT 1320 GCGGTGCTGG GTTCAAAGAT TTAAGTTCAA CGAATTTAGA GACAGGCTAG TCTGGGAAGC 1380 AGAGCAGGGA ACACTGCAGC CCACCATGTG GGAGTCTTGG GCGTGGGTGG GACGGTGAGG 1440 CAGGGGCCTC ATGAGCATTG GAATCCTTCC GCGAAGGAAA TCAGGGAAGG TTCTGGATAG 1500 GAGAAGAATC TCTTGGCGCT GTATTTGAGG AAGGTGTCAG CAAGAAGCAG TCCTGGAGCA 1560 GGGAGGGAAG GGCGGCCGGA ACCAGTTAGG AGATTGTATC TCCTGACCCA GGAAGCCGCT 1620 CTGCATTATT CACGGCCACT CCCCTGCCCT TCTCTACCCC AGACCTCCAT GTGGGATCTG 1680 GCCGGGGAGG AGCTGCCGTG GGGGGTGGCA GCTGTGGGAG GAAAGAGGAC AGAGTCACAT 1740 GCCGAGGACT CATCACAGGT GTAAGATGTC CTGGTTATGC CTCAGCCCTC GACAAACACT 1800 CCTGCCTCCC TGCTGTTGTC TACCTCAATT TAGAGACGAG GTCCAGCCAG ATGGCCTCAA 1860 AGATCCCGGC CCTGCCTGTG TTTTTCAAAG GAAGCCAAAC CTCAGATTTG CCTCAGAACT 1920 TGTACTTTTC TTCTAAGCAA ACGCCGTCCA CCACGAGAAC CGCCTGGCAT TTGGCTGGGA 1980 AAGAACAAAC TGGAAGCTTG CAATTTCCAG GCTTAATTGC ACAGTTCCTT ATAATATTAT 2040 TATATAGAAC TTTTATTGCA CTGAGAAAGC CCAAGCGTTT CCTTTTCCTA TTTATACCTG 2100 AGCCCAGTCT CTCCTCTGCT ATCATTTCCT CCCTTGCCCA CTGCAGAAGC TGATGGCTGT 2160 TTGGTTCCCT TTCCAAAGAG AGGGCAATTA GGATGTGAGT TGGAAACTCA TTTGTCCCCT 2220 TTGGTTGACT CGTGGAATAT CAGTCAATTA CCACATGTTA TTGATCACTC ACCATATGCT 2280 TGACTGGGCT TCATGCTGTG TAAGTCTATA GAAAATACCT GCTTTAGAGG GGCTTCTGGC 2340
|