Tag | Content |
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EnhancerAtlas ID | HS076-16906 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr13:113991820-113992650 |
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) |
KLF13 | MA0657.1 | chr13:113992051-113992069 | CCAACGGGGGCGTGGCCC | - | 6.38 | KLF14 | MA0740.1 | chr13:113992054-113992068 | ACGGGGGCGTGGCC | - | 6.24 | KLF16 | MA0741.1 | chr13:113992056-113992067 | GGGGGCGTGGC | - | 6.62 | MSC | MA0665.1 | chr13:113992003-113992013 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr13:113992003-113992013 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr13:113992003-113992013 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr13:113992003-113992013 | AACAGCTGTT | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I113337 | chr13 | 113991961 | 113992110 |
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Enhancer Sequence | ATATAGAGTT CTTTTAAAAA AAAGTAGCTT ATGGCGAAAC CTGGTATCAA GAGGCCTCGG 60 ATTGTACAGC GTGCTTTCTG CGCAACCCTC TCACGGAATA AGCTCACACT TAAGGTGCAA 120 GGCCTGAGGC CCACAGGTCT GGTGAGCCTG GCCGCCTGGT GACTCAGCGC AATCTGATCC 180 CAAAACAGCT GTTCCTGACC CCAGAGACCA GCCTCCTGTG ACAAAGCCAG CCCAACGGGG 240 GCGTGGCCCA GGCCACATGA GCACCACCCT CAGGACAGGT GACCTCAGGG AACCCCACTC 300 GGGAGGACGC AGGAAACGCA CCTCCGATGT GGCAATTGCG GCGCCAAGAG CCTCCCTCCA 360 CCCACCTCTG CTCACGGGGC TGAGCCGTGG TCCCCACAGA ATGTGCCTTG TCGGTCCACA 420 TCTCAGCCAG TCCTCCCAGC CAGAGCTGAG GTATTTCTAT GTCGAGTTGT TAAAACCTGA 480 CCTGCTTCCC TATTTTTCAG AGGAAACCAG GTCAAACCCA TCTTTCAGGA TGTAGAGCGC 540 TAATTCAGGG CTGCACCGAC TCATGACTGA CGCAGTCTTC CGAGACAGGG CCCCCTCCAC 600 CCTCAGTCAC GCGGCAGGGC CCGGTCAACC TCCTCCTCTG AGGAGGCCCG GGACCCATCG 660 CCCGCCCGGG GAGCGGCGTC TGCACCTTCT TCCTGCGTCC TTTCCATGCC TTGTTGGGAT 720 GGTGATTGAT GGCCATCATC TTCATGGGCT CTACAAGAGG CCGCGGGTGT GGCAGGTGTT 780 CTGGGCTGAG AACTCGGGGT GTGGGGCATC TGCGTGTGGA TGGTCACAGG 830
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