Tag | Content |
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EnhancerAtlas ID | HS111-01363 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr13:109917710-109918850 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr13:109917710-109917720 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr13:109917710-109917720 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr13:109917710-109917720 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_35939 | chr13:109915848-109918374 | HMEC | SE_35939 | chr13:109918425-109919081 | HMEC | SE_65014 | chr13:109917698-109918388 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I109263 | chr13 | 109915693 | 109921242 |
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Enhancer Sequence | ATTTTCCATT ACCTTCCCAA ATCCTATAAA ACGGCCCCAC CCCATCTCCC TTCGCTGACT 60 CTCTTTTCGG ACTCAGCCCG CCTGCCCCCA GGTGAAATAA ACAGCCATGT TGCTCACACA 120 AAGCCTGTTT GGTGTCTCTT CACATGGACT CGAGTGAACT TTGATGCCGT GGCTCGGATC 180 GGGGGACCTC CCTTAGGAGA TCAATCCCCC GTCCTCCTGC TCTTTGCTCC ATGAGAAAGA 240 TCCACCTACG ACCTTAGGTC CTCAGACCAA CCAGCCCAAG AAACATCTCA CCAATTTTAA 300 ATCCAGTAAG CCGCCTCTTT TTACTCTCTT CTCCAACCTC CCTCACTATC CCTCAACCTC 360 TTTCTCCTTT CAATCTTGGC GCCACACTTC AATCTCTCCC TTCTCTTAGT TTCAATTCCT 420 TTCATTTTCT GGTAGAGACA AAGGAGACAC GTTTTATCTG TGGACCCAAA ACTCCAGCGC 480 TGGTCACGGA CTGGGAAGGC AGCCTTCCCT TGCTGTTTAA TCATTGCAGG GACACCTCTC 540 TGATTATTCA CCCACGTTTC AAGGGTGTCA GACCATGCAG GGATGCCTGC CTTGGTCCTT 600 CACCCTTAGC GGCAAGTCCC GCTTTTCTGG GGAAGGGGAA AGTACCCCAA CCCCTTCTCT 660 CTGTGTCTCT ACCCGTTCTC TGCTTTTCTG GGGAAGGGGC AAGTACCCCA ACCCCTTCTC 720 TCTGTGTCTC TACCCCTTCC CTGCTTTTCT GGGGAAGGGG CAAGTACCCC AACCCCTTCT 780 CTTCTTGTCT CTACCCCTTC TCTGATTTTC TGGGGCAGGG GCAAGAACCC CTCAACCCCT 840 TCTCCTTCAC CCTTAGTGGC AAGTCCCACT TTTCTGGGGG AGGGGAAAGT ACCCCTCAAC 900 CCCTTCTCCT TCACCCTTAG TGGCAAGTCC CGCTTTTCTA GGGGGCAAGA ACCCCCAATC 960 CCTTATTTCC ACACCCCGAC CTCTTATTTC TGTGACCCAA TCCCTTATTT CCACACCCCA 1020 ACCTCTTATC TCTGTGCCCC AATCCCTTAT TTCCATGCCC CAACCCCCCT TCCCACTTTT 1080 CTAGGGGGCA AGAACCCCCA ATCCCTTATT TCCACACCCT GACCTCTTAT CTCTGTGCCC 1140
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