Tag | Content |
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EnhancerAtlas ID | HS055-00453 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr1:116657140-116659540 |
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) |
Klf1 | MA0493.1 | chr1:116658773-116658784 | AGGGTGTGGCC | - | 6.32 | MEF2B | MA0660.1 | chr1:116658386-116658398 | GCTATTAATAGC | + | 6.14 | MEF2B | MA0660.1 | chr1:116658386-116658398 | GCTATTAATAGC | - | 6.14 | ZNF263 | MA0528.1 | chr1:116658440-116658461 | TAAGGAGGAGGAGGGGAAAGC | + | 6.36 |
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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 |
GH01I116115 | chr1 | 116657699 | 116659217 |
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Enhancer Sequence | CTCCAAAGGC CGAACGTCCT CTGCCAAACT CCTCTATATC TCTGCAAACA CATACTAAGC 60 ACCTGCTTTG TGCAAAATAC TGTGCTACGG TTTGAGGGTA GACCAAGGCC TGAGATGTGG 120 CCTGCTAAAT GAAAGAGAAA TTTTGGTTTT GGTCTCTAGG ATAGCCCTGT CCCATCTGCA 180 GATTTTGTAC ATAACCCCAA AGGAAGAAGG AGGGAATTTC ACATGCAGTC AGGCAAGTGC 240 TTAATAGAAT GCATGGTAGA CCGTAAGGGA TGCAGTAGAG ATTTCAACAG ATTGCTGGAG 300 GAGCACGGTG CATTAGTTGT GATGGGAAAG GTGTCTTACA GAAAGAAGAG TAGAGACAAA 360 GCCTTGGAGG AAGTGTAGGG TTTTAATAAG TGGAGAAGTA TAGGAAAGGT CTTCCAGGCT 420 AAGGGAACCC CGTTCAAACA TTCAAGGTGT ATTTCATTCC CAGTCACCTT TTTCTTTTGG 480 GGAGCAGAAC AGGGCAGTGG TTACAAATAT GGGCTTTGGA AGGCTGCTAC CTGTGTTCTG 540 TAACTTACTA ACTTTGGGAA CCTGGGCAAA TTACTTAAAT ATTCTGAACT TTGGTTTCCT 600 CATCTATAAA ATGGGGATAA TCATAGCATC CACCTTAAAG AATGATGGGT AGGCAGGAAT 660 GAGCCTACTC TTATAAAATG CCTTGCACAC AGGAAGGACT AAATAATCTT AGTTTCACGG 720 TAATGCTGCT GCTACAGCTT CTGCTACATT TGGGGGCTGC AAATATTCTG CGTGACCCAA 780 GCATTTGATT CATGGAAGAA TTAGTCTACA AAGGAAGGGA TATGATGGTG GAAAGCCTAT 840 GGTCTCGTGC GTATCTATCA CTGGATTTAA CTTTCCATTT CTTTACATTA TTAGCCCCTG 900 AAAGACAGAG ATGATGCCAG TTTTTGTTTT GTTGAAATTT TTCTAACTGA TGATTGGATT 960 TCATGCAATT CTGGAATTAA AGGTCTGACT TCTTGTTTTC TGGAAGGAAG TCCTCAGCCT 1020 TTTCTTCTCA GTAACACTCA TTGGGAATGA CATACACATA GTCTGCATGG TCATGGGTGT 1080 GATCAGGCCT GTGTGACATT CCTGGCATGC TACTTAGCAC CACCACTCTG TCTCCATTGC 1140 AAGGAAGCGT ATCGGAATGC AAGTGAGTCA GAGTGATATT ATTATAGGGG ATAACCTTAA 1200 ATCCCCATAA TTTATATTTG AAGCAGTAAA TTATTCATGA ACTTGAGCTA TTAATAGCAG 1260 CAAATGACTT GTGGGGCAAC AATGAACCTG ATGCTGTGGT TAAGGAGGAG GAGGGGAAAG 1320 CAGCCCAAGA TGGGACAAGG ACCTTGACAG CATGGAGACA TGCCTGGGAA GAGCAAGGCC 1380 CAAACAACAT TTGTTTCCAT GTTTTGCCAT GAACTAAGTT TGGTGACAAG GTTGCCTCAA 1440 GGCTGCCTTG AAGCTGCAAC TGGTATCTTG CTGGCTTCCT AAAGTTTGAG AGGCAGTAAA 1500 GGATTTCCAG GGTTGGGCTT GCAATGGGTG TCTACTTGTG TTAGAGCCTC CTTCTTTAGA 1560 TCACTGTACA GCTGCCCCAA CCCCACTGCC TGCTTTTCCA CACCCTGAAA TGAACTTCTT 1620 GCTGTATCTG TCTAGGGTGT GGCCAGAATA AGTGGAGAGA AACAGTCTGG GGGTTCTGTG 1680 TTGTCACACC ATGAGGGTGA CAAGAGGTGT CTGGCACTAA GCCTGGAAAC CCCCAGCACA 1740 AATCACTTCT GGGGCTACCA AATAGCACGG TGATGCTGTG TGGGTAAGAA CTTATTGCAG 1800 GAAGTGTAGC CAGAGATGTG GGGAGGGACA AGGCTGCCCG CCACCTAGAG AAAGAGGCTT 1860 CTGCTCAGGT CCCACAGCAG GAGCATCACT GTCTGGCCCT TGCTGCATGA CCCTTTGTGC 1920 TTGTTAGATG CCAGAACAGT TGCTGATGCC TAAATACATG GAGACCTAGG ACTCCTTATT 1980 TCATGAGTCT TGACTTTAAA TTGAAGGCAT TTTTAGGTTC AGGAAGAGGA TAAAGGGTAG 2040 GCCGTACTTC TGGTACATCA GTACTTAAGG GTGTGGCAAA GTGTGATGGA AAGAAGTGTT 2100 GGAGAGCCTG TCTAATTCTA CATCTAACTG CCGGTGTGAT GTTAGGAAAG CTGCCTTGTC 2160 ACTCTGGTCC TCCATAAAGT CACACCAGAC GAGGCAATTT CTGAGGTCTC TTCCATTTCT 2220 AAGATCCTGA ATCTAAGTTG CAGCAGAAGT GATGGAGGAA GAAAATTAAA ACTGGAATTT 2280 GTGGTTCTAG GTCTCAAAAA GCATTATCTT ATTCTGACTT TCACCTTTGG TAATCAAAAC 2340 AGGTCATAAG GGTGAACTAA TAACCTGTGT AACAAGTGAG AGATTATAGT TGTTTTCCAG 2400
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