Tag | Content |
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EnhancerAtlas ID | HS078-04808 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr12:132014090-132016140 |
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) |
NFYA | MA0060.3 | chr12:132014560-132014571 | GGCCAATCAGA | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr12:132015449-132015464 | GAGGTCAGGAGTTCA | + | 6.22 | REST | MA0138.2 | chr12:132015270-132015291 | ATCAGCACCAAGCACAGCAGC | + | 7.08 | TCF3 | MA0522.2 | chr12:132014811-132014821 | AACACCTGCT | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I131529 | chr12 | 132014283 | 132014643 |
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Enhancer Sequence | GTATATACTA TTATTATTTG TCAATTAAAA ATAAAATATT TTGGTTTGGG TGGGAGTTGC 60 AAGAAAAAAA ATTAACTTTA ACTTGAAAAT CAGAAAAGAA ATGGGATCAG GAACAAAAGA 120 CCCACAACAA GCAGAACATC GGTACCGGCA AGGCGCCCTC CTCACTGTCC CTGGGGGTCC 180 TCCGCAGGCC ACAGGAAGGG CAAGGGAGCC TGTCAGGCAT TCTCCACACC TTCGGGCCTC 240 GCTTTGGGGG TCCAAGGTCC TCAGAGGCAC GGATGTGGAA CCACGGAGGG GACAGGGCAG 300 GCTCTGCTGC AGGCACCTCT TCTCTTCACA GAGACCCCCC ACCCCCACCA CGCCCTTTCT 360 GTGGTTGGGT GCTGACCCCA CAAGGGGGTC ATGTGATGCA GGCCTGACCA ATCAAGCGAC 420 TCCATCCCGT TTCCAGTGAT TGGTTCTGGG ACAAACATGT GACCCGCTGT GGCCAATCAG 480 AACCAGACTA GGACTTGCAC AGGGAGCGCT GGGAAAGAGC CTCCCTCTCT ATCCGGGAAC 540 CTCAGAGCTG CAAGTGGGCA CCACTCGCTT TCACGTGTCC ATGCTGGGAG AGACCTGGGA 600 TGGATCAGAG CCCAGATGGG GGCTAGGCAA TGGGTCAGAG CCAGGACAGG AGGTGCCACA 660 AAGTGGGGGT ATGGGGTCAC AAGACCAAGC CGATGCAGAA GATCCACCGA GGCTGAGCAG 720 AAACACCTGC TACCTCCACT GAGCCTGGAA CTGGCCGCCC CTGATCCCCC ACCTTCTCAG 780 AACTTAAGTC CTTTTACTTA TGGGAGTTGA AGCTGATCTG CTATTCTTTA AAAGCTTCCT 840 CTCTGTAATT GTGTCACTTG AAGAATATTA CACAAATGGA AGCATTCAGC CTGGAGCATT 900 TTGAGACCAG CCTTTTGCAC TATTCTCTTG CAATCTGTCC AAGTTGTTAT GTCATCAGAT 960 GGGAGCCGTC CTGTTGCTTA CAGTCAGGCG AAGCTGTTCT CCTGGTGAAC CCACACTTCA 1020 CGGAACACCT GGATCACACA GAACCATCTG TGACATGAGG AAGCAAGACA AAAACAAGAA 1080 CAACTGTGAT CATATCAGAT TACAGACAAA ACACGAGCAT GTTCCAAACC ACAAAACAAT 1140 CAACGTTCCC TCTATCTTGG CCAGTGTGAG AGACTGCAGC ATCAGCACCA AGCACAGCAG 1200 CAGCCTTGCT CTGCTCTTCT TAGCTTCAAC CTAAGAATTG TTAAGGTGCC TGTCTTCATC 1260 CATTTTCTGC TGCTATAACA GAATACCACA GACTGGGACC AGGCACAGTG GCTCGCACCT 1320 GTAATCCCAG CACTTTGGGA GGAGGTGAGC GGATCACCTG AGGTCAGGAG TTCAAGACCA 1380 GCCTGGCCAA CATGGCAAAG CCCTGTCTCT ACTAAAAAAA AAAAAAAATT GGCCAGGCAT 1440 GATGGTGGGT GCCTGCAATC CCAGCTACTA GGGAGGCTGA GGTGGGAGAA TCGCTTGAAC 1500 CCAGGAGGTG GAGGTTGCAT TGAGCTGAGA TTATGCCACT GCACTCCAGC CTGAGTGACA 1560 GAGTGAGACT CTGTCTCAAC AACAACAACA AAAAAGGAAT ACCACAAACT GGGAAATTTA 1620 TAATAAATAG AAGTATATTG GCTCAGAGTT CTGGAGTCTA GGAAGTCCAT TATGAAGGTC 1680 CTGGCATCTG GTGAGGACTT TCTTGCTGTA TCATAACATG GCAGACAGAG AGAGGAGGTA 1740 AACCACCATA ACAGCATGAA TCCGTTCATG AGCTGAACAC CTCTTAACAG CCCCACTTCT 1800 CAACGCTATC ACGAGTTTTG AAGGGGGCAA ACATTCAAAC CATAGTAGTG CTTAATCACA 1860 GAAATACTCC CCGCTTCCTA ATAGCATCTA ATTCAGAGAA ACTCCACTTT CTTAAACCTC 1920 CCCCCAAGTC ACCTAACACA GGTCCAAGTC CTACGCTAAG TGCTTTTGAT GCTGTCTTAC 1980 TGAGAGGTCC ACACTTCCCC AAGGTATGTG TTCTTCCTCA CCGCAATACA TCAGTAAACT 2040 GAGTTTATTA 2050
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