Tag | Content |
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EnhancerAtlas ID | HS002-06866 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr3:64094490-64096070 |
Target genes | |
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) |
FOXH1 | MA0479.1 | chr3:64095586-64095597 | TGTGGATTGGA | - | 6.62 | ZNF263 | MA0528.1 | chr3:64095263-64095284 | AGGGGTGGGGGAGGAGGGGAG | + | 6.17 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I064109 | chr3 | 64094738 | 64096095 |
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Enhancer Sequence | GGTTTCCCAA CCTCAGTACT ACTGACATTT CGGGCTGGAT AATTCTTTGT TTGGTGGGCT 60 GTCCTGTGCA CTTCAGGATG TTCAGCAGTA TCTCTGGACT CTACCCACTA GATGCCAGTC 120 ACACATCCCT CTGGTTGTGA CAGCCCCGAA ATGTCTCCAA ACAGTGCCAA ATGTCCCTGG 180 AGGGCAAAAT CGCCCCCAAC TGAGGACCGC TGCTCTAACA GATCCTGTCC TCCACCTGCT 240 GCTTGACCAT AGCCCAAGGG GAGCTCTGTT CCTGTCCACC CAGTTGTTGG AGTGAGTTAA 300 ACCTGCTCTA CCCCATCCTG CAGACAGGAG CCTCGTCACG ATGGGGGTTG CCGCTCCTTC 360 TTTCTAGAGA AGGATTATCA GGGCTCTGCC TGGTTGGGTG TGGTATGTCC CCAAAACTGG 420 GGAACTCTAA AAGTTATTTT CTCTCTAAAC TCTTCTCAGA AAATTCACAT TCCTTTCTCT 480 CAGTGGCTAT CAAGAACTCC CCAGTTAAGG CCTTTGCTGT CTAATTTTCC TGGCAGGTTT 540 GAAGCTTTTG AAATCCTGAG TTTTTGATGT ATCTCTTTTA CTTCCTTACT CCAGCCACTG 600 GCCTATCTAG CAGGTCTCAG GTGATCAGCA GATCACAAGT TGGCTTGCAG TCAGTTACAC 660 ATCTGTCATC TGCTCTGGTG CTACCAGGAT CAGTGCTGGT AGTCTAAGGA ATGATTTCCT 720 CTGCCAGCTG CACTGGGGAA GGGAAAGGGA AAGGGGAGGC CAAGCCCTGG GGCAGGGGTG 780 GGGGAGGAGG GGAGTGTGCA TAACTTCTTA CTTCACACTC CCACCCCCAG GCTTGGCCTG 840 CCTTCCCTCT CAGTCAGGCA TGGGCTGTTT AGGCCCAAAC TAAATAACAG CCTCTTTACA 900 ACCAGCTGCT TCCAAAGAGG GTCATGGACT GATCTTGGTT TTCCCAACAA TAGCGGCTTT 960 GTTTTTTAGC AGCATTCATT CTAGGGACTT GCCTTTGAAC TGGAGGTTGG GGAGTGACAA 1020 GCATTATAAT GGGACTAGAA TCACTTCTCT GACAGACCCA GTACAGTTAC AAGGACAAGT 1080 CAGATAAAAA CTTGAGTGTG GATTGGAGGT TTCTTACCTT CTATCCCTTT CCTTGCTCAT 1140 CCTATTAACT TCCGGATAAA TCAGTGACCC CAATAAAGAT GGAGTCAATT TTAACTAAAA 1200 CCACTTGTAA AAGTGAAGGA GGAAACCAGG AAGGGACATC TTCCAGAATC ATGTGGAGTC 1260 AGTTTTAACT AGTACCACTC AGCTCCATGG GGGATTCTGG TTGTATTGCC ACAAAGCATA 1320 TTGCTAATTG AAAGGATACA CAACAAATTC AGACCAGTTG AAGATTTTTT TGCCAGAGTT 1380 TGCTCTGGGT TTACACTGAC CCCATGCTGC TTTCTAGAAC CCATTAGTCT GGGTCAACAA 1440 GCAGACCATG CTGTATTTAC TTGGGAAACA CTTGACTACA GGAGGACAAA AGCTAAATGG 1500 CTCCCAAGTG GTAGAGAGTG GGCAGCCAAG AACCTGGGGA CCCACTGAGT TGCTTCAAAG 1560 ATCTTTGACA AAGCCCTGCT 1580
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