Tag | Content |
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EnhancerAtlas ID | HS041-13648 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr21:42582290-42583240 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr21:42582645-42582656 | CTTGAGTGCCT | - | 6.14 | ZNF263 | MA0528.1 | chr21:42582861-42582882 | TTCCCCAACCCCTCCTCCTTC | - | 6.69 | ZNF263 | MA0528.1 | chr21:42583092-42583113 | CCCTCCCCATCCCTCTCCCCC | - | 6.91 | ZNF263 | MA0528.1 | chr21:42582858-42582879 | TCCTTCCCCAACCCCTCCTCC | - | 7.25 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 42582350 | 42582939 | chr21 | 42582557 | 42582705 |
| Enhancer Sequence | ACTAATGTTA AAATAGAGAA TAGAACAGAC TGTTTGTGGC AACAAGATAC CAACTTATAA 60 GCAGCAACCT CAGGTCACGC CAGGCAAGGG TTGAGCCGCG TACTCTACAC TTAGAGAACG 120 GATTCTGTTC TCATGGCACA GCGTCTTCTT TTTCTCCAGC AGCTAAAACA CTCACCGGCC 180 CGGAGATCAG CCAGATTCAA ATGACTGCAG CTCATCCGCC CACAGACGCA GACTGACCCC 240 GTTCCACAGC CATGACTGCA GCTCGGATTG GGCAGGAGAC TGACTTCAGG AACCTCCTCC 300 AGATAAGAGA CCCCTGACAG TGGACTGGCT CTGGTTGCTT TACAGAGGCT GCTCACTTGA 360 GTGCCTTCAA GTCCTGAAAA GACCTTTTTG ACATTTAGGG CCTAACTGTG ATACACTTAA 420 ATGTTAAGAC TCCAGCCCAG AGTGAACACA GGAGGCATGT CACATGGATG TTCAATATGC 480 GTGCATCAGG ACCACCTTCA TGAATATTCA TAGTTCCTCC TGTAAACTGC TGAATATGTA 540 TGTTTAGCCA ACCCATTCAG CGTAAAGCTC CTTCCCCAAC CCCTCCTCCT TCAAAGTGCC 600 TGTCTCTGTT CTTGCACAAA GGCACACTTC CCAGACTGCA GGATGGCCGC CTTGCACCTT 660 TATAAGAAGG TATTCTTTTC ACCTTCCCAA ATGTATAAAT ATTGTGTTGA TTTTTTTTTT 720 AAGTGAACAC TGCTAAATGC TAAGCATTTG GTGGAAAACC ACCACATTCC AGAATCAGGC 780 AGCCAAGCCC ATCCCCATTC CCCCCTCCCC ATCCCTCTCC CCCCTTCACT GCCACCGTCC 840 ACTTGGCAGC TGTGGTTTTC CCAAGAGGAG CCCAGGTATC CATGTGTCTC TCAACATGTG 900 TCTTTCTAGT AGGAGCCTGT ACAGCAATAG TGAAATGGCT CACACTCTCA 950
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