Tag | Content |
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EnhancerAtlas ID | HS105-25862 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr14:101539270-101541930 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr14:101539709-101539722 | ATGACATCATTAC | - | 6.48 | JUND(var.2) | MA0492.1 | chr14:101539708-101539723 | AATGACATCATTACC | - | 6.2 | Myod1 | MA0499.1 | chr14:101541689-101541702 | TGCAGCTGTCCCT | + | 7.82 | NR2C2 | MA0504.1 | chr14:101539588-101539603 | AGGGGGCAGAGGCCA | + | 6.05 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I101070 | chr14 | 101537262 | 101542129 |
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Enhancer Sequence | TAAATATGTT TGTGTGTCTG TATGTTCGGA GATGATGTTT GTTAAGCGGG AGGTTTAACA 60 ACGGAGGCCA TCTGCCTTCA GCAGGGATTC GCACAGAATG TCACTGGCCT TCGCCCAACA 120 AGCACTTTGC AGGGAGCAAC CTCCTGAAGT CGGGGCTCAC TCCTGGGTCC CCCTCCACTG 180 CATGCGAGCC CCCCGTTCCA AGGCAGGAGC CAGGGTCACG AAAATGCATG CTTCTTCATC 240 AATCCGAGGT CTCAAACGGC TCCCCCAGCC CCACTGCCTG CCCGTTCCAG GCCTGGGGCT 300 GGCAGCCTGG GCCCCACGAG GGGGCAGAGG CCAGAGCCCG GCGGCAGAGC CCGTGCCCAC 360 GCCTCGCTGC TGCCAGCCTC CGCTTGGTCA CGACACAGCC AGGCTGACTC AGACACAGCC 420 CCAAGCGGGA GCCTCATAAA TGACATCATT ACCTATGAAA CCTGCCGTGT AGTGCGCTAG 480 CAGGGAAGGA CACACTCTGG CCGCCCGGTG ACTCACACTG TTTTCCCCAG AGCCTTCCTG 540 CTCCACCGCC TGGGTCTGAG CTGGCTGGGC AGGGGGAGGG GGCACTCAGC TTGGCCTCAC 600 TCCCCCGCTC TGCTGCAAAT GCAAAAGCAA TCGGCCAGGC AGCCACCATC CTGCTGAGGG 660 CTGTGTGTGG GGGTGGCGGG GAGGAGGGGG GGCACCATCT CTCCGGCCTC CCTCTGCAGC 720 CCCAGTGGCG CTCCAGAGGG ACTGTCAGTT GCCTATGACA GGGGAGGAAA CTGAGGCCTA 780 AAGAGGCCCA ATGCCTGGCC TCACAGATCC CACAGGGGAG GGTGGCTTCG GCTCATGCTG 840 GGAACCCCCA GGGAGACCCT TCGGCGAACC CAGCCGCTGG GCAAAGCTGC AAAACCTCTG 900 GCTGTTCCTG CTGGGCCTGA GACTCCAGCT TCTCCTGAGC TCCTTTGGTG CAGCCAACTC 960 CTCCTGCTGA AAAACACTTC TACTCTTGAA AGTGGTGGCC TTGCCAACCC AAGATGTCCC 1020 CACCAGGTGG GGGGCACTGT AGGGGAATGC TAGTTTTTTT TTCTTCAATT AAAAAAAAGT 1080 AAAACAAATA AAATGGGACC TGTTGGGTAT GGCCTTCAGA GTCGGAGGAC TTGGGTTAAG 1140 ATCCAGCCTT TGTCATTTAC TGGTACTGTG GTTTTCTTGT ATCTGGCCTC CACCTCCTAG 1200 GCAGGATGAG AGTTAAATGC CTGTTAGGTT CACGTTAAAC TGGGGCTCCC CCTCAGTGAT 1260 CCATGGTTGG GGAGGACCCC CACCAATCCT GAGGTCGCTG TGCACCTGCA GCCCAGACCT 1320 CACCCTGGCC CGGGGACCTG GCCTGATGGT CCAGCCCCCC ACACACTGCT GGCTCTGGGG 1380 CTGTGCCCTC CTGATACGCC CCCAGCACCT GATGGCATCC CCCAAACAGA ACAAGAACCG 1440 CAAACAGCAA CAGCCCGTTT TTGCTCTTAG GAAGCTCAGA GCAGCATCTA TGCCAAAATC 1500 GTTCACACTC TGGTCCCCGG AGCTACAGGT CACAAGCTGG TCCTCACCCA GACCCGCTCC 1560 TCAGCAGCCT CCATCCCTGA CCCTGGTTTC CTGGGGACTC TGCTCCGCTG ACTTCTGAGC 1620 TGTGGGAGCT GTAAGGGAGA GGAGTGGGCC ACAGACTTGA TGGGAGGATA CAGAGGTAGA 1680 AATTCAAGTC AGGGCCACAG AGTTGTGTTC AAAACTGGGA ACATGACCTG GGCTTGGCAC 1740 AGAGCCTGGC GCCTGGGATG AGTGGAGAGG GAGAATTGGA GGGCACTGGG ATTGGTAATC 1800 CTCAATGCAT CTTAGGCAAA TGAGCTCGGG GTCACAGGGC AGGATACATG GGACCAAGGA 1860 ACACTGGTCA GCCATCAGTG CTGTGACCCA GGTGGGCTTG AGGTACAGTG GGGGGTCCCA 1920 GGACTGGCAG GCCCCACAGA GTAGCCTTCC CTGAGTTTGT CTGAGCCAAA AATCCCAGCA 1980 AAGGGCTTTG TGGCCCGTTG CCACTTTCAC CCTGGTAGCT CCACCCCATC TCCCCCTTTG 2040 CCATGAACTC ACAGCTCTCC TGCGAGGCCA CAACCCATGC CAAGACTTTC AATGGGTTAA 2100 GGAATGTGCA CATCTCTAAA TGACCACACG TGCCCTGTCA TGTACACGTG CACACACACT 2160 GACATGCATT TGAGGAATGG GGGCATTCTC TGTGCCTGAG CAGAGGCCAG GGACCCTGGA 2220 TGGGTAGGAA AGAGTCGAGG GAGTTGGGCA GCAGAAGCAC GTGCTGGTAG GGATGGCAAG 2280 GAGCCCTGGA CGTTGGTGGT GGGTGGGTGC TGTATCAGGA CCTGGGCTAG AAGAAAGGCT 2340 TGGGATCAGA GTGGACCCAG TTCTCTTTGA AGCATAGCTT TCTTCTGGTT CTTTGTAAGA 2400 CCAAAGCAAC TGACACCTGT GCAGCTGTCC CTGGGTGACT TTGTCTGATA TCACACAGCC 2460 ACAGGACTCT CTCTCTGTCC CAGTCACTAC TGAAGCTGAC TCTGCGCTCT CTCCCCGGTG 2520 ATGAGGCCTC TCTTCTCACA GATGGGTGAT TTCTCACTCT CATCCAGTTC CCCTCCTGGC 2580 CACACTCATT TTCTTATTGA GGCGCAGGGG GTACCACCCC TGGTTTGGGG ACTGTTCGGC 2640 TGGCCACACC CCCTCTTTGG 2660
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