Tag | Content |
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EnhancerAtlas ID | HS105-69022 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr6:42766010-42767480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr6:42766130-42766140 | TTTAATTAGA | - | 6.02 | HES2 | MA0616.2 | chr6:42767174-42767184 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr6:42767174-42767184 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr6:42767252-42767267 | TGATCTCTTGACCTT | - | 6.93 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH06I042799 | chr6 | 42767002 | 42769200 |
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Enhancer Sequence | CCCAATCCCC ACCAGTATGC AATATACCCA TGTAACAAAT ATGCACATGT ACTCTCTGAA 60 TCTAAAATTA AAATAAATCT AAAAAAGAGT CACATAAACT AGAAAAAGAA AAAAAATTTT 120 TTTAATTAGA AAAAAAAAGG TGGGCCGGGC ATGGTGGCTC ATACCTGTAA TCCCAGTACT 180 TTGGTAGCCC AAGGCAGGCA GATCACTTGA GGCAAGGAGT TTGAGACCAG CCTGGCCAAC 240 GTGGTGAAAC CCCGTCTCTA CTAAAAGTAC AAAATTAGCC AGGCGTGGTG GCAGGCACCA 300 GTAGTCCCAG CTACTCGGGA GGCTGAGATA GGAGAATTGC TTAAACCCAG GAGGGGGAGG 360 TTGTAGTGAG TTGAGATCAA GTCACTACAT TCCAGCCTGG GTACTGTCTC TAAATAAATA 420 CATAAAATCA GAAAAAAAAT TGTGTAGTGT TTGCATATAA CCTACACAGA TCCTCCCATA 480 TACTTTAAAT CATCTCTAGA TTTGTTTTAA TTTTTATTTT TTATTACTGC TCCTTGCGGA 540 GCGTGGCTAC CCCATAGGCA GCATGCCCAG AGTAGCCAGT CATTTCTAGA ATATTTACAA 600 TATCTAATAC AATGTAAATG CTATGTAATA GTTGTTAGAC TATATTGTTT TAAAATTTGT 660 ATTATTTTTT ATTGTTATAT TGTCATTTTT TGTTTTACTT TTCCTAAATA TTTTCAATCT 720 GTGGTCATTT AAATCTGGGG GTGCAGAACC CATGAATATG GAGGGCTGAC TATATTAACA 780 GTGCCTGGAA ATTTTTTACC CAGTAGAAAT ATGTATTAGA CACAAGGTCT CACTATATTG 840 CCCAGGCTGG ACTTGAACTC CTGAGCTCAA ATGAACCTCC TGCCTTGGCC TCTCAAAGTG 900 CTGGGATTAC AGGCAGGAGC CACCATACCT GGCTGAAATA TTTTTATATC ACATTATACT 960 AGCAGATATC TTGAAATATT ACTGTCTTCC AAATGAGGGT AGTTATTAGA TTCACCACTA 1020 AATCTTTTTT TTTTTTTTTT TTCTGAGATG GAGTCTTGCT CTGTCACCCA GGTTGGAGTG 1080 CAGTGGCGCG ATCTCAGCTC ACTGTAGCCT CAGCCTCCTG GGTTCAAGGG AGTCTCCTGC 1140 CTCAGTCTCC TGGCTGGGAC TACAGGCACG TGCCACCACG CCCGGCTAGT TTTTTGTATT 1200 TTTAGTAGAG ATGGGGTTTC ACCGTGTTAG CCAGGATGGT CTTGATCTCT TGACCTTGTG 1260 ATCCATGAGC CTCAGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC TGCACCCAGC 1320 CCATCACCAC CATTCTTTTC CAGAAGTGTT CATCTTCTCC AACTGAAACT ATGTATCTCA 1380 TGATCTCTTG ATACAAATAA TTACAATACA AATTCCAGTT CACATGGCAT TTCTTAGGAT 1440 TTATTAAAGA TTTCAGTAGA TAGAAGTTTA 1470
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