Tag | Content |
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EnhancerAtlas ID | HS108-00783 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:24132430-24134620 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:24133163-24133175 | GTATGTTTGTTT | + | 6.37 | GFI1 | MA0038.2 | chr1:24132509-24132521 | CAAATCACTGCA | + | 7.22 |
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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 |
GH01I023807 | chr1 | 24134101 | 24134250 |
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Enhancer Sequence | GAGCCTCTTT TTTTTTTTTG ATAAGAAGTC TCACTCTGTT GCCTAGGCTG GAGTGCACTG 60 GCGCCATCTC AGCTCACTGC AAATCACTGC AACCTCCACC TCCCGGGCTC AAGTGATTCT 120 CATGCCTCAG CCTCGCAAAT AGCTGGGATT ACAGGCTCAC GCCACCACGC CCAGCTAATT 180 TTTATATTTT TAGTTGAGAC AGGGTTTCAC CATGTTGGCC AGGCTGGTCT CAAAACTCCT 240 GACCTCAAGT GATCCACCTG CCTCAGCCTC CCAAAGTGCT GGGATTACAG GTGTGAGCCA 300 CTGTGCCCAG CCGAGGAGCC TCTCAAACGG AACATTTCAG ATCATCTCCC TCCCCGCCCC 360 TGCTCAAGAC TCTCTGTTAG CTTCCCAGCT CAGTCTGAAA GAGTCAAAGT CCTACAAGGC 420 CCCCGATCTG GCCTTCCTCT AACCCTGACA TCTCTGCCCC CCTCTCCTCA GTCACACTGC 480 TCCCGCCACA TGCCTCCTCC TGATCCCTGA ACACAGCAAG CACACTCCTC CCTCAGGGCT 540 CTGCGCCTGC TTTCCTGGGT GGGGCTCCCT TCCCTCCCCC TCCCTGCTAG GGATCCGCAG 600 GGCTCACTCC CTCGCTTCCC TCAGGTCTCT CTCAAATGCT ACCTTCTGAG TGAGGCCACT 660 CTACAGAAAG GCCTGGCACT GCCTTAACCT GCTTCATTTT TTCTCCACAG TGTTTATGAA 720 CACCTGGCCT GCTGTATGTT TGTTTATTTA TTATCTGTCT CATAGTACTA GAGTGTCAGC 780 CTCATGAGGG CAGAGACTCT GTTTTGGTCA CAGCTGAATC CTTAATGCTG AGAACAGTGC 840 CTAGCACACT AGGCACCGTT AGGTTAGGTT TTAATAGGTG AATAAATGGT CTTACAATGT 900 GCTATTTACA CGCCTGTAAT CTTCCATCTG TCTTCCCCAC CCACCATAAC ATGAGCTCCC 960 AGAGGGCAGG GATTGGGTCT TGTTACCATT GTCTAAGTCA GCACTTAACC TGGCACATCG 1020 ATCCATATTT CCGAAGTAAC TGATGGAAGA GGGAGGTCAG AGGAAGCTAC TGCCAGACGT 1080 CACACAGCTC AACCTGTTCC CTGATAAATT TTCAAAAAGG GGATTCTGAG ATATCACTGC 1140 CATGAAACAG AGAAGCACAG AGGAGCAGGA GTGTCCTGAG CGTGATCAGG ATGAAGTTTT 1200 GCCTCAGACT CACCTCAGCT GTGCAGAATT CCCCTTTACC TGCCTGGCAA GGCATAGGAG 1260 AGGAAGTCAC TCTTCCTGTC TGCCTGGCTG GGAAACGCAT GAGCTGAAGG AAAGCCCAGG 1320 AACCAGGGCA GGGTATCACA GTAAGCTGAA AAATGAGGAG ACCACAGAAC TACGAACCTT 1380 AACCTTGACA GCCACAACTC TGAGGAAACC GACCCAGAAC ATAACAGACT CACCTGGCTT 1440 AGACACGAAC CTCTAGGGGA TAATTGAGAG GAAAAAAAAA GTGGCTGGAA CTGCCATCAC 1500 TATCCTAGAG ATGGAAGGTT AGGCCAATGC TACAGCAAGG TAGCTGTGGT CAGACACTAA 1560 GAATGCTCCT TCTATCTGGC TGCCAGCCAA TGGATCTCCA TTCTGGACCA GCCCACGAGA 1620 AGCAAACCTC AAAGGAAACT AATCTGAGGT CTTAGCTCAA TCTGTGGGGA ACGGCATTAA 1680 AGCCTCTCCC TCTGAGTGAC CTCTGCTAGC TTCTCTACCT CCTGCTTCCT CATCTGCTTC 1740 TGCTACACAC CCGCACACTG AAAACCCTGT ATATTGTATG AGTCCTCCCT GAACCCCACA 1800 TCAGTCCTGA GGTGCAATTC TGCCTAGTCA TCTTTCCTCT TCCCTCAACA GCAGCTTACT 1860 TTATGTTCTT CAAGCTTCAC TGAGGCCTCT TTTGCAAATC CTCCCAGATC TCCTCAGCTG 1920 GGATGGGGCC CCTCTAGGCT TCCTGAGCCC CATGCTTCCT CCCTTCATGG CATCTGTCAT 1980 AATGCAGTGG GATTGCCATG TAACTCCCTT GACTGTCTCC CCAACACAGA GCTGTACACT 2040 TCACATCTGG GCAGGGTCAC CATGACTGTG TCCACCATTG CCAGCTTGGA ACCTGGCATA 2100 CTGGCATCAG TAAATGTTTG CTGAAAGAAT AAATGATAAC AAGCTGTCCT GCCCACCGTG 2160 ACCTTTGGGA GAATGGGCAT ATGCTTTTGA 2190
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