Tag | Content |
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EnhancerAtlas ID | HS034-08570 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr13:113991720-113992590 |
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 |
|
Enhancer Sequence | CTTGAATTCA GCAATTTGTT AGCATACAAC TCAATTAAAC TTTATCTGCT ATAACTAGGA 60 GACCCTGAAT GGAAAAGCGG CAATGACTTT TTTCCCTAAT ATATAGAGTT CTTTTAAAAA 120 AAAGTAGCTT ATGGCGAAAC CTGGTATCAA GAGGCCTCGG ATTGTACAGC GTGCTTTCTG 180 CGCAACCCTC TCACGGAATA AGCTCACACT TAAGGTGCAA GGCCTGAGGC CCACAGGTCT 240 GGTGAGCCTG GCCGCCTGGT GACTCAGCGC AATCTGATCC CAAAACAGCT GTTCCTGACC 300 CCAGAGACCA GCCTCCTGTG ACAAAGCCAG CCCAACGGGG GCGTGGCCCA GGCCACATGA 360 GCACCACCCT CAGGACAGGT GACCTCAGGG AACCCCACTC GGGAGGACGC AGGAAACGCA 420 CCTCCGATGT GGCAATTGCG GCGCCAAGAG CCTCCCTCCA CCCACCTCTG CTCACGGGGC 480 TGAGCCGTGG TCCCCACAGA ATGTGCCTTG TCGGTCCACA TCTCAGCCAG TCCTCCCAGC 540 CAGAGCTGAG GTATTTCTAT GTCGAGTTGT TAAAACCTGA CCTGCTTCCC TATTTTTCAG 600 AGGAAACCAG GTCAAACCCA TCTTTCAGGA TGTAGAGCGC TAATTCAGGG CTGCACCGAC 660 TCATGACTGA CGCAGTCTTC CGAGACAGGG CCCCCTCCAC CCTCAGTCAC GCGGCAGGGC 720 CCGGTCAACC TCCTCCTCTG AGGAGGCCCG GGACCCATCG CCCGCCCGGG GAGCGGCGTC 780 TGCACCTTCT TCCTGCGTCC TTTCCATGCC TTGTTGGGAT GGTGATTGAT GGCCATCATC 840 TTCATGGGCT CTACAAGAGG CCGCGGGTGT 870
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