Tag | Content |
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EnhancerAtlas ID | HS055-01107 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr10:65557840-65559690 |
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) |
Foxd3 | MA0041.1 | chr10:65559308-65559320 | GTTTGTTTGTTT | + | 6.32 | NKX2-5 | MA0063.2 | chr10:65558836-65558846 | CTCAAGTGGT | - | 6.02 | RUNX1 | MA0002.2 | chr10:65559063-65559074 | AAACCACAGAC | - | 6.62 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I063798 | chr10 | 65558106 | 65559974 |
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Enhancer Sequence | TGCAGTGGCG CGATCTCAGC TCACTGCAAC CTCTGGCTCC GAGGTTCAAG CGAGTCTCCT 60 GCTTCAGCCT TGATGTCTGT AAAATCTATC TTGAAGAAAG GTGGAAATGT TGGGGAGATT 120 AGAAAAATAG TACTGTCACC CCACAGGTGC TCAAGAAACG ATAGTGCTGC ATAATTTTTT 180 GTGACAGGAT GGCTCTTTGT TCTATGAGGC ACAAGGCAGG CATGACAAGT GTGAGACACC 240 CTTGGGAGTC AAAAAATATT TTAGGGAGGG CTGAGTTTAC TGGATCAGTT TACCATTGTG 300 AAATAAAAGT CCTTGGACTC CAACAGGGTT TGGAGTCCCT CTCTCTGAGT GTTTTTTAAG 360 GCATGGATTA TTCTGTCTTG ACCACATTTC TAATCTAGTA ACCACAGCCT CATCTCCACT 420 TCTTCCTGCT TTGAATTTTG TCCTCCAAGG GCCACTTAAA TGAGAAGCCT GTCCCACTCA 480 CCTTGTCTAG CATTCAGTGT GTATCTCATG CCACCTCTCT GCACTGACCT AATCCATGTT 540 GACCATTTTC TGTGTTTCAG AAGATGGACT CAGCTTAGTA CCTGGCACAT AACAATAATC 600 CCAAAGACCT TGATGCTCAG AGATGCCTGG GCTAACTTAT TTATCTTCAG GCCACTGTCT 660 TCACAATTAT ATAACCACAG GGGAGAAAGC CAAGAGCATT GTTACAGGAT CTCTGGGTTG 720 TAATGTGATA GGCGTCCTTT CAACATGGCA TCTATGGAGC CATAGATGTT GTGCTGGAAG 780 GAGCTTGGAA GTTCATTGAG CCTAGCCTTG TTGTTTCAGT AATAAAAAAA AACTGAGGCA 840 GAAGTGGGTA GAAGAAATAT CTAGAAGTAG AAGCCAGGTC TCCTGGTTCC CAGGACAGGG 900 TCCTTTATAT CCTATCCCCT CTAGGCTGTA ATATATAGCA ACGGTAAAAT ACAGACTCAA 960 CTTTCTCGGT CTTACAAGTG GCAGGCTGTT GCTGGCCTCA AGTGGTGAAT CCACTGATAG 1020 GGAAAAATAA GAATTTTGTA AACTCTCAGA AAGTTCGTCT TTGTAATAAC AGTCCCCTAA 1080 ACTCTGTTGT TCTTGGAAGT ACAACAAAGT CCAGGCTGAG ACCATGGAAC TGGACTCAAG 1140 TCAGGATTTA TGTCACACAG TCTATGTATT TCCCACTCAG TGCCAATTAT TCATTCCTCC 1200 CATTCAAACG AAAATAAATA ATAAAACCAC AGACAGCGAG CAGTGTGAAA AAAGCCTTGA 1260 CTGAGAGTGG GAAAGCTATG ACCATCCTGT GAAAACATTT ACTTCCTGGA GAGAGATCCA 1320 GCAGTACTGT GTGTTCCTTC CGGGGGTGGG GCTGGAGGCT GCCTGACGTG ATGGGAACTT 1380 AAATGTAAAA GAGGTAGCTG TGTCGTATCT TCTTTGTTGA GAAGATAAAA GTTCATTCAC 1440 TGGGAAAAAC AGCCGCAGCT CCTTTTTTGT TTGTTTGTTT CTTCTTCAAC TTTTATTTTA 1500 AGTTCAGGGG GAAATGTACA GGATGTGCAG GTTTATTACA TAGGTAAACG TGTGCCGTTG 1560 TGGTTTGCTG CACAGATCAT CCCATCACCT AGTAAGCCCG TCATCCAGCA ACCATTAGCT 1620 GTTCTTCCTG ATGCTCTCCC CCGCTTCCCC CTCTGACAGA CCTCAGCATA TGTGTTGTTT 1680 CCTGCTATGT GTCCATGTGT TCTCATTATT CAGCTCCCAC TTATAAGTGA GAACATGCAG 1740 TGTTCCTTCT AAGGTGGTAT TTCCAACACG TAGAATGCTC AGGGAGGGAA AGTCAGAGTT 1800 GGATGCATAC TATAGAAGGG TTGCAATCTA TTCCGATACC TCTTCCCAAG 1850
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