Tag | Content |
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EnhancerAtlas ID | HS108-29490 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:184067330-184068370 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arntl | MA0603.1 | chr3:184068117-184068127 | GCACGTGACC | - | 6.02 | GLI2 | MA0734.2 | chr3:184067664-184067679 | CTCCGTGGGTGGCCT | - | 6.32 | PHOX2A | MA0713.1 | chr3:184067956-184067967 | TAATTCAATTA | + | 6.14 | Phox2b | MA0681.1 | chr3:184067956-184067967 | TAATTCAATTA | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | ACTACAGGTG CCCACCACCA TGCCCAGCAT ATGCTATCTT TTAAAATTCA TCTCTCAGTA 60 TAAGTAGTAG GAGTAGTAAC AGTAATTCCT AACATATATT GAGTATTTAC TGTGTGCTAG 120 GCCCTATTGT AAGTGCTTCA CATGTTTCAA GTCCTTTAAT TCTTAGAAAA CCCAGTGAGG 180 TGTGATCCCC ATTTTACAGA TCGGGAAAGT GAAGCACAGA GAGGCTAAGA AACTTACCAA 240 GGTACACAGC AAGCCAGCAT GTGGCAGAGT AAGGATTTGG GTTCAGTTGG TCTGGCCCTA 300 GCTGTGGCCG CCACTCTGGC CTTTACCATT GCTTCTCCGT GGGTGGCCTC TGAATGAATT 360 ACTTATTAGC CGGCACAGCG ATCTCCAGTT GCACGGGTTC CTAAGTAGTC TCCAGTGTTT 420 TCTCTCTCTT ATCTGAATGT TCCCCTCCTG AACTTAATTG GGCGACTACC TATTGATTCC 480 TCAGGCCTGT AAGGACATTT TGAATTCTAA TCTTTTATGT TCTTATCACT TCTAGTTCTT 540 TGTACTTTTG TTAGTTGGTT CCTCAAAGAC TTCTTCTCTT CTGATTTTTA AGTTTGTAAC 600 AAATATCTAC TTTGTTCTTT TTCATTTAAT TCAATTAGAC ATCATGGAAC CCATTGGAGG 660 GCCCATACTT CTTGGGCCTG GGAACAGTGA ACTGACATGG AGAGGGACAA CATGGCCTTC 720 TGAAAGAATC CTGGGAGCAG GGCCAGGAAA TCTGGGCTCT GGGCCTGACT CTGCTGTGCT 780 GACTCAGGCA CGTGACCTCC TCGCTGCATG CCTCAGTTTC CCTGTGTATT AATATGGTTA 840 AGGCCACAGG CTTTTGAGTC AGACCATCCT AGATTCCAGG CCCAGTTCTG CTACTTATTA 900 TTATTTTTTT GAGATGGAGT TTCGCTTTTG TCACCCATGC TGGAGTGCAG TGTCATGATC 960 TCGGCTCACT GCAACGTCCA CCTCCCATGT TCAAGCAATT CTCCTGCCTC AGCCTCCCAT 1020 GTAGCTGGGA TTACAGGTGC 1040
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