Tag | Content |
---|
EnhancerAtlas ID | HS073-03829 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr13:109782550-109785020 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr13:109784252-109784266 | AAGAAGTGACTCAG | + | 6.17 | Myod1 | MA0499.1 | chr13:109784636-109784649 | TCCAGCTGTCCCC | + | 6.02 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH13I109131 | chr13 | 109783474 | 109784722 |
|
Enhancer Sequence | TGTAAAATTT AGTTTCTTGG ATCCTAATTT TGTCTCATAT GTGACTATAA GGTACTTAGA 60 GATGCGTTTG GTCCACTGTG TCGCACCCTG GTGAGCAGAC CTTTCAGAAG CTTGTCAAAG 120 GGCAAGTGTA TGCATTGTTT CCTTTTTACC ATCTACATTA TCTGTTCTTT CTTACAGTAC 180 ATAATTCTTC ATGCTGGTTA CTTTACAACC ACCACCACAA AAAGAAAGTC TTTGATCTCC 240 TGCAACTAGA GATGTATTTC TGCATTCTGG CATGTGCTCT CAATACTGTA TATTTTTAAG 300 AATAAGACAA TTAACCAGCT TAAGCTGCTT GAGCATGCTT GCTGATTAGT TTTTACAGCA 360 TTAGGGAGTC AGAGAGGGCA AGCGCAGGAG CTTAGCCACT CAGTCTGTCA GTGGTCTGGG 420 TTTGTAATCC ATGATCGCAA AGGTAGCTCC ACCCACACGT GATAAGCCAG CTGTCAGACA 480 GGGTTCTGGT CCCTTCTGTG CCATTATGTC AGGAGCTGAA GGTGGTTGAG TTAGGACAGT 540 GATGAAATTG ATCCTAGCAT GTTAGACATC TCCCTCAGTC CAACACAATC CGAGTATAAT 600 CTAAGTCTTT GTTGTTCAAT GCAGTAGCCA CTAGGCACAC GTAGCCAATT AAGTTTAGAG 660 TAAATAAAAT TAAATACAAT TTTAAATTTC ATTCCTCCAT CATCAGTCAC TTTCCAAGTA 720 CTCAGTAGCC ACAGGGGTAG AATTTTTCCA TCATCACCGA AGCTTCTCTT AGACAACCCT 780 GATTCTAAAT GCTTTGTGTG TCTACCAAGC GGTGATACTG AATTTTTTGC ATCTAGTAAC 840 GTGTCACAAA ATTATTCTCC TTTCTGTCAA AAGATAGGAA GACCATTTGA TCACTATTCT 900 AAAATGTTTG GTGAACCTTG GTTTCGCAGG ATCAAGGACT ACGGCTGAAG TTGGTTTTGT 960 ACCTGAGCCA TCCTTTTTGG CATGTTAAAA AATCAAGTTC AAGTTCTTTT CCTTTACAAA 1020 TAAAGCTGCG AATCAATTCA GATGGTTACA GAGTGAAAGG AGATCTGATC GGAGACCAAG 1080 GGCCAAGGAT TGTAGGGTGA CCAGCACCAC GGTCACTTCA AAGTTGTCTT TGTATTTATT 1140 CTTGTTCTTA CTAGCATATG TCTTTCCTGG TAGGTCTTCA CCCAATAAAA ATGGTTGTGG 1200 TGAAGGAAAA CAGTACAGAG AGCAATTTTT TCTCATTTCC TTTGTGCCTC AAAAGCGTGA 1260 AACAATTTTG CAGGCCAATA AATGTTAACA CTTCTTTGCA AACTACCAGC AAGCTAGAGA 1320 CAACTTTTTT TTTTATTATA CTTTAAGTTT TAGGGTACAT GTGCACAACG TGCAGGTTTG 1380 TTACATATGT ATGCATGTGC CATGTTGCTG AGACAACTTT TTAAAAGTAC TATGTTTTTG 1440 TTAGGTCAGT GCAAAAGGAA TTGTGGTTTT TGCCATTGAA TAAAAGCCTG CAGTTGCTCT 1500 TTGCAAATAG TGGCTAGGAA AGGAAAGATA GGGCCTCGTT TTCACTTCCT CTTGGCTGGG 1560 GCCTCCCAGC TGGAGTGCTG TTCTGCAGAG TTCATTCCTC ACACACCGGG TGCAGCCTTT 1620 CTCCCAAAGA CGGTTAACAT TCTCTCGAAT TGTCTCCTGA CTGAAGTTAA ATATAAGCCT 1680 GCATTTCATG CGTGTGACTT TGAAGAAGTG ACTCAGTCTT TCCAAGCCCA TGTATGTCAA 1740 GTAGCAGCAA CAGCCGAGAC ATGGCAAGGG CTATTTCTGG GGAGTTAAGA AGCAAAGGAC 1800 TGTAAAGCCT CATTGCCCAG GACGTAGCAA GCGCACAGCA AAGTTACATG CATATAACTT 1860 TGTTGTTAAT GAAGCCTCTG ACAGTCAGTT TCCTCATCTG TGAAATGGAT ACTAAATCCT 1920 AAGATGTGGG ACTTGCAATT AAGTCATGAT GTCAGTGGTG CTGTGCCTGG CTTGGAGTGA 1980 CGGTTGCTCA AGGTGAAATT GCAGAAGCAA GCTTTTCTCA GGCAGCTCTA GTCCTCACTG 2040 TTCACCGTTC TATGTTGATG CTTCCACACT CACCCTCCCT TCAGACTCCA GCTGTCCCCT 2100 CCTTGGGGAT CATACCTTAA TGAAACCATA ATTGTTTTTT CCAAAATTGC TGTACAACTG 2160 CATTCTCCAC AAAACACAGT TTACATGTGT AGACACAATC ATGGCTCAGC TCTGTGGCTT 2220 AATTTGGAAA TAATATGTCT TTTCTTTACT CTCTTGTTTC TGTCTTCATT CTAGAACAAC 2280 ATGTGTCACA TAGTAAGCAC TCATCAAATA CTTACCAAGT GAATACATGT TACAGAAATC 2340 TATTTCTCTA CACTCTCTTC ATTAAAAGAG AATTTGCTTC CTATCGGTAT ATGAGAGGGA 2400 GCACAATTTG GCAAGGTTCG AGAAGTACCC TTGAAATGTG TCAAGGCTAG ATTTGTCTGC 2460 ATATTTTTAA 2470
|