Tag | Content |
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EnhancerAtlas ID | HS037-24748 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr3:48180800-48183590 |
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) |
EWSR1-FLI1 | MA0149.1 | chr3:48183520-48183538 | CTTTCCTTCCTTCCTTCC | - | 10.53 | EWSR1-FLI1 | MA0149.1 | chr3:48183524-48183542 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr3:48183528-48183546 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr3:48183532-48183550 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr3:48183536-48183554 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr3:48183540-48183558 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr3:48183544-48183562 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr3:48183548-48183566 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr3:48183516-48183534 | TTTCCTTTCCTTCCTTCC | - | 6.2 | EWSR1-FLI1 | MA0149.1 | chr3:48181955-48181973 | GGAAGTGAGGCAGGAAAG | + | 6.45 | EWSR1-FLI1 | MA0149.1 | chr3:48183552-48183570 | CCTTCCTTCCTTCCAGAC | - | 6.49 | LMX1B | MA0703.2 | chr3:48181677-48181688 | TTAATTAAAAT | - | 6.62 | Myod1 | MA0499.1 | chr3:48183211-48183224 | GGGGACAGCTGCT | - | 7.04 | Nr2f6(var.2) | MA0728.1 | chr3:48181184-48181199 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr3:48183520-48183541 | CTTTCCTTCCTTCCTTCCTTC | - | 6.48 | ZNF263 | MA0528.1 | chr3:48183524-48183545 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr3:48183528-48183549 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr3:48183532-48183553 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr3:48183536-48183557 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr3:48183540-48183561 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr3:48183544-48183565 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 48182591 | 48182651 | chr3 | 48181800 | 48182272 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I048140 | chr3 | 48181891 | 48182090 |
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Enhancer Sequence | CCGTCTGTAC TAAAAACACA AAAAAATTAG CTGGGTGTGG TGGCAGGTGT CCGTAATTCC 60 AGCTACTCAG GAGGCTGAGG CAGGAGAATC GCTTGAACCC GGGAGGTGGA GGCAGGAGTG 120 AGCCGAGATC ACACCATTGC ACTCCAGCCC AGTCAATAGC GCAAGACTCC ATCTCAAAAA 180 TAATAATAAT AAAAAAATAT ATAGGCCGGG CTTGGTGGTT CACACCTATA ATCTCAACTC 240 ACTGGGAGGC AGAGGTAGGA GGATTGCTTG AGGCCAGAAG TTCAAGATCA GCCTGGGCAG 300 CACAGCAAGA CTACATCTCT GGCCAGGCGC GGTGGCTCAC GCCTGTAATC CCAGCACTTT 360 GGGAGGCTGA GGCGGACGGA TCACGAGGTC AGGAGTTCAA GACCAGCCTG ACCAACATGG 420 TGAAACCCCC ATCTCTACTA AAAATACAAA AATTAGCTGG GCATGGTGGC GCGTGCCAGT 480 AATCCCAGCT ACTTGGGAGA CTGAGGCAGG AGAATCACTT GAACCAAGGA GGTGGAGGTC 540 ATCCGTGGTT GAGACCCACT GTCTCCTTTT TTTTTTTTTT TTGAGACGGA GTCTCGCTCT 600 GTCACCCAGG CTGGAGCACA GTGGTGTGGT CTCGGCTCAC TGCAAGCTCC GCCTCCCGGG 660 TTCACGCCAT TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG ACTACAGGTG GCTGCCACCA 720 CGCCCGGCTA ATTTTTTGTA TTTTTAGTAA AGCCAGGGTT TCACCGTGTT AGCCAGGATG 780 GTCTCGATCT CCTGACCTCG TGATCCGCCC ACCTCAGCCT CCCAAAGTGC TGGGATTACA 840 GGTATTAGAC ACCACGTCTG GCTCATCTTT TTTTCTTTTA ATTAAAATTT AAAAATTAAA 900 AAAAAATAAT CATATGGACA AACCCCTAGA GAGCAGAGGA AGGAATAATT AACACTGCCC 960 AGGGGAGTCG GAAGAAGCTT TGGAGGAGGA TTGAACTGAG AGAAAAAGAT TGGCAGGAGT 1020 TTGTTGTGCA AAGAAGGGGA GGGACAGGTG TTTCACCGGA GGGAGCAGCA TGTTCAGGGA 1080 CACACAGCTG TGAACAGGCA AATTGTTGAG GAACGCTGAG AAGTTTGCCT GGACCCGAGG 1140 ACGAACAGGG AGGCAGGAAG TGAGGCAGGA AAGGCCAGTG GGCAAAACGG AACATGAGAC 1200 CTTGCTGTGA CCTTCAGACA ATCTAAACTG CTTGAGAGGT TGAGAAGCTT TGCATTTGGA 1260 AGGGAAATTA GCATTTGTGC TGAGAAATAA AGCCGTGCAT GGAGCGACAA CTCTGTGTCC 1320 AGAGCTTTAC AAGCATTTGC TCTACATCAC AATAAAGTGT GTATTTCACA GACAGGGACA 1380 CAGAGCTATG GTCTTTCTGC AGTGCAAGCT CTCTGCGAGC AGGGAACACG ACCCCAGCAC 1440 AGCCCTACCA GCTCCTTTGA GGGTGAGGAC ACCCTCACTT GGGAAGAAGC AAGTTGGAGC 1500 TTTATTTTAT TTATATATTT ATTTAATTAG TTATTTAGTT ATTTATTTAT TATTACTATT 1560 GAGACAGGCT CTCACTCTGT CACCCATGCT GTAGTGCAGT GGCGTGATCT TGGCTCACTG 1620 CAGCCTCCAC CTCCCAGGCT TGGGTGATCC TCCCACCTCA GCCTCCCTGG TAGCTGGGAC 1680 TACAGGCATG AGCCACAATG CCTGGTTAAT TTTTTGTATT TTTTGTAGAG ATGGGTTTGC 1740 ACTATGTTGC CCAGACTGGT CTCAAATTCC TGAGCTCAAG TGATCTCCTG GCCAGCACTG 1800 TGGGAGGCTG AGGTGGGAGG ATTGCCTGAG TTTGGGGAAG TTGAGGCTGC AGTGAGATCA 1860 TGCCACTGCA CGCCAGCCTG GGCAACAGTG TGACACCCCA TATGAAAAAA ACAAAAAAAC 1920 TGTTGGATGA AGTTTTCTGT AAATATTAAT AGTTATTTTA GTTGTCTCTT GGCTTTGGCC 1980 AGCACCTTTG GGGAGTATCT CCCAGGCTGT CTGTGGTTCA CCAAAATCAT GTGGAAAAGG 2040 AAGGGGCTCC ATTCACTCAC TTCCATAGTG ATACCCAGGG TGAGAGTGCT CCATAGAGCA 2100 CTCCCCCGAC AGGCAGGCTG CTGAGGGAAG ACTTCCTGGA GGGCAAGAGG CCTAGATGAC 2160 CCAACTAGGA AGAGAGGGAG AAGTGGAGGG GTAGAGTGGG AGATGAGCTC AGGAATGAGG 2220 GCAGGGTCTG GTGGAGGCTG CTTGGAGAGG CCACTCAGAG GGAAGAATAC CTGCTCCTGG 2280 CTCTGCCTGT CACCTCTTGG TTCCTTGTTT CCTCATCTGC CTCAGCAGGC TTCTCTGACC 2340 GGGTGGTGGG CAGTGGGAGA GGGTGGAGGA ACGACCTTCG CCTCAGCCAG AGTATGGGGC 2400 AGGCCCTCTG TGGGGACAGC TGCTTCATGG CTTAGCCTTA GCTGATTATG GTGGCCTCAC 2460 CATGCCTGTC TGTCCATCTG GAAAATGGGC TCAATAATGG TATCTGCCTC ATAGGGTTTC 2520 ACGAGGACTC GAGGGAGATG ACTTTTGCTG CTGTCTTGAT TTTGTCTGTT GTTTTTGTAG 2580 TTACACAGAG GATAACAGAT GAATCAGACA CTGAACCTGC CCAACCCTAT GTGCTGGACT 2640 CATCATAATC ATACCTGGGA CTTTTGAGAA CTTACTGGAA CTGTGCTACG TACCCTATAT 2700 GTATTAAGTC ATTTAATTTC CTTTCCTTCC TTCCTTCCTT CCTTCCTTCC TTCCTTCCTT 2760 CCTTCCAGAC AGAGTCTCGC TTTGTCGCCC 2790
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