Tag | Content |
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EnhancerAtlas ID | HS146-00573 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:61803470-61804530 |
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) |
Mafb | MA0117.2 | chr1:61803603-61803615 | AAATTGCTGACT | + | 6.92 | RUNX3 | MA0684.1 | chr1:61803677-61803687 | AAACCGCAAA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64290 | chr1:61802112-61805213 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I061336 | chr1 | 61802364 | 61805416 |
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Enhancer Sequence | AGCACCCACT CTTTTGTTTA TTTTGCGCTA GTGTTTTCCT CAAAGTATGA GTGCTAAGGC 60 TGTCAAATAT CACTCCTGGT AGGAACCCAG AAAGTTCTCC TGAAAAATCC ACTACTTCTG 120 CCCATTTCCT TCCAAATTGC TGACTCTATT TTACTTGAAG TTGGTGGAGT GACTTCGAAA 180 CCCTAACTAC TTCACTGGGA AAGAGGAAAA CCGCAAATAC ACACAGGCCA TTGTGACTCT 240 GGCCTGGTGG GCTCTAATTT TCTAGCGGCG GTTTGTACAC CCAAGCCGGC TGCAAGGGTT 300 AAGTAAACTT CGTGGCTAAG GATGACTTCA TGGCCCTGGA ATTTTGAAAA GCCAGGATTC 360 TCAGTACACT GTGGCCAGCC TTAGAGTCTT TGGGTGTGAA AACCACTCTC AGTTACCCGG 420 ACTGATTTTT GGTTCCTGTT GCAGTGCTGC AGAATCTATT AAAATCCGGC AGCTGAATTG 480 TCCTGGCTCT GCCACAAAGC TCAGCTGCCG GGTCCACTAC AGGATTCCTG AGTTGTTTGT 540 CAATGGAGAG TGGGAGTGAA TGGAACCAGG CATATGCCTC AGCCTGGCAT GAGGTGGCAC 600 CCTAGTGGCT GTTTTCTGCC TTAGAAATGT GCGCTCTTTC TATATTTTCA CACAGGAATT 660 GTCATTAACA TCCAAATTGC AGTTCATTTC TAAAGTTCTT TTTGAAGTCT CTGGGTCCTT 720 GTTACGTTTT CAAGTACCCA TATTCAGATG CTTAGATTTT CAGGCTAGTA ATTTAGTAAG 780 AACTATTGGC AATATTCTAA CCTGACATGG TGGAACTTCT AAGACAGAAT GAACTCGGCT 840 ACAAGGCACA ACAAGAAAAC GAAACTCTTG GGTAGGAACA AGCCCAAACT TGAAAATACA 900 AAATGTTCTT GCACAGAAGG ACTAATGAGG AAATGGGTGT AGGATAAGAA ATTCCAGACA 960 TCCAGTCATT TGGGGTGCCA TTTAAACATT CGCAGTACTT TAGATCTTAA TTAAAGTGGG 1020 ATAGATTTAA AACTTTCTTT CTAAACTAGT GGCCTGTTGG 1060
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