Tag | Content |
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EnhancerAtlas ID | HS091-28105 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:172410010-172411030 |
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) |
IRF1 | MA0050.2 | chr2:172410443-172410464 | TTACTGAAAATGAAAGTACAC | - | 6.55 | NFYA | MA0060.3 | chr2:172410621-172410632 | AACCAATCAGA | + | 6.62 | NFYB | MA0502.1 | chr2:172410616-172410631 | AAAGCAACCAATCAG | + | 6.7 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I171553 | chr2 | 172410481 | 172410630 |
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Enhancer Sequence | GTAAGTTGCA TAGTCTTCTT AATTGTAATA CTTAAGCCAC AAAATGTTAA ATACTTGTTC 60 ACTGGGAAAA TGTAATAAAA ATATAACAAA ATTTTTTAGA TATTAAAATT AAAAAATATT 120 TTAAAGAATT TGTTATATCA TATAGGTAAT ATGATATTAC TAAAAGTTTA GAAGGACCAA 180 AAAGTCTGAC AAATTGTATT ACTCTTATGA AACAACTATT GAAGTTATAC ATTCCCTTTC 240 AATCTTGTTG ATATGCATGT TTTTATATTA ATTGTAATTA TAGTGTACAT ACATTTTTGT 300 TTCATCCTTT TTAAAAATTT TAAGTGATAA CTGTTACTGG TGGAGGGTGT CCAGGTTCTT 360 GGCGTTTTGA ACAAAGAAGT GGACAAAACA CACAAACAAA GCAAGTAAAG AATGAAGCAA 420 CAAAAGCAGA GAGTTACTGA AAATGAAAGT ACACTCCACA GGGCGGGAGT GGCCTGAGCA 480 GCCACTCAAC GGCCCGATAG GGAATCTTCT TGGGTCCAAA TAGCCCCTAG AGGTTTCCCA 540 TTGGCCAGTT GGTGTTCACT GCATGTAAAT GAAGTGGTGG CCTGCAGTCA GTTTGATTGG 600 TTGTAGAAAG CAACCAATCA GAGATACTTT CAATTTTCCA TCCGCCATGC AGAAAAGCGG 660 GGTTTGCAAA GGGAGTAGCC TCGGGTCCTT TTGCTACTTA GATGTGGAAA GTTGGGGTTT 720 TCCTTTTGGT TTAGTTCTAG GAAGTCCGTG TGAATTGACC TGAGGTTGCC TGCCTCCAGA 780 CCCTACCTGC CTTAAAACAA GTGTTACAGA TGCTATATTA TTTTCATATT TATTATTTTT 840 AAATCAATTT CATTATATAT TCCCGAGTGA ATTGTAGCAT AATTTATATT TCTCCTTAAT 900 AGCAAGCTTT GAGAGTTTAC ATTGAAACTG TACTAGTGTG CATTTTGAGC AGATAAATTC 960 AAGACTGTTT TGCATGTTGC TGTATCATCC TGTTTGTAAT TGGATACATC TCTTATTTCA 1020
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