Tag | Content |
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EnhancerAtlas ID | HS044-07305 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:102842920-102845140 |
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 | chr2:102843224-102843242 | AGAAGGGAGGAAGGGAAG | + | 6.05 | EWSR1-FLI1 | MA0149.1 | chr2:102843104-102843122 | GGGAGGGAGGAAAGAAAG | + | 6.23 | EWSR1-FLI1 | MA0149.1 | chr2:102843228-102843246 | GGGAGGAAGGGAAGAAAG | + | 6.25 | EWSR1-FLI1 | MA0149.1 | chr2:102843127-102843145 | GAGAGGGAGGAAGGAAAG | + | 6.42 | EWSR1-FLI1 | MA0149.1 | chr2:102843232-102843250 | GGAAGGGAAGAAAGAAGG | + | 6.62 | EWSR1-FLI1 | MA0149.1 | chr2:102843236-102843254 | GGGAAGAAAGAAGGAAGG | + | 6.72 | EWSR1-FLI1 | MA0149.1 | chr2:102843081-102843099 | TAGAGGAAGGAAGGAAGG | + | 6.84 | EWSR1-FLI1 | MA0149.1 | chr2:102843077-102843095 | GGAATAGAGGAAGGAAGG | + | 7.01 | EWSR1-FLI1 | MA0149.1 | chr2:102843085-102843103 | GGAAGGAAGGAAGGAGAC | + | 7.67 | ZNF263 | MA0528.1 | chr2:102843245-102843266 | GAAGGAAGGGAAGAAAAAAGA | + | 6.06 | ZNF263 | MA0528.1 | chr2:102843141-102843162 | AAAGGAGAGAGGGAGGGAAAA | + | 6.09 | ZNF263 | MA0528.1 | chr2:102843090-102843111 | GAAGGAAGGAGACAGGGAGGG | + | 6.17 | ZNF263 | MA0528.1 | chr2:102843216-102843237 | GATGGAGGAGAAGGGAGGAAG | + | 6.25 | ZNF263 | MA0528.1 | chr2:102843106-102843127 | GAGGGAGGAAAGAAAGAGAGA | + | 6.3 | ZNF263 | MA0528.1 | chr2:102843226-102843247 | AAGGGAGGAAGGGAAGAAAGA | + | 6.64 | ZNF263 | MA0528.1 | chr2:102843713-102843734 | AGAGCAGGAAAGGGAGGGAAA | + | 6.65 | ZNF263 | MA0528.1 | chr2:102843094-102843115 | GAAGGAGACAGGGAGGGAGGA | + | 6.7 | ZNF263 | MA0528.1 | chr2:102843132-102843153 | GGAGGAAGGAAAGGAGAGAGG | + | 6.94 | ZNF263 | MA0528.1 | chr2:102843229-102843250 | GGAGGAAGGGAAGAAAGAAGG | + | 7.06 | ZNF263 | MA0528.1 | chr2:102843219-102843240 | GGAGGAGAAGGGAGGAAGGGA | + | 7.12 | ZNF263 | MA0528.1 | chr2:102843222-102843243 | GGAGAAGGGAGGAAGGGAAGA | + | 7.12 | ZNF263 | MA0528.1 | chr2:102843129-102843150 | GAGGGAGGAAGGAAAGGAGAG | + | 7.51 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 102843334 | 102845009 | chr2 | 102844840 | 102845062 | chr2 | 102844003 | 102844653 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I102226 | chr2 | 102842670 | 102846324 |
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Enhancer Sequence | TCTCTCTAGG CCCTGTACTT GGTGCCTGAA GGGATTTAAG TCTTCAACTC TCAGATATGG 60 AGAGAGATCA AACCAAGTTT GAATGTGACT TCTCCACTTA CTCCCTATGT AAACTTAGAA 120 AGATGTTTAA CTTTCTTCTA TTTCTCAGCT ATAGAAAGGA ATAGAGGAAG GAAGGAAGGA 180 GACAGGGAGG GAGGAAAGAA AGAGAGAGAG AGGGAGGAAG GAAAGGAGAG AGGGAGGGAA 240 AACGGAGGGA AGAAGGGAGT TTCGTAGAAA AGAAACTAAA GAAAGCAGGG GAGAGAGATG 300 GAGGAGAAGG GAGGAAGGGA AGAAAGAAGG AAGGGAAGAA AAAAGAAAGA AACAAAGAAA 360 GGGACAGTGA TTAAATCCTG CTTTTTGACA GTGGGAATAA CTGAGTTGAA GTACAGGGAA 420 GCATTCAGCG GGGCCTGGGC CACAGGGCGG CCTCTATTGC TTGTCTGGAG GTCAAAACAA 480 ATCCCCAACA CCACAGCTGT GGGTTTTAGT CTGTGGGCCT ATGTCCTGCC AGTGCTGTTT 540 GGCATAGAAA TGCCTCAGTG TGATCCTGAC TCTCTGAGAG CCTGGCATTT CCCACCATGG 600 TGCTTGTGAC TATGCTACTT TTGTTTTGTT TTGTTTTGTT TTGTCTTAGA ACAGATACAA 660 TCTATTAAGG CCTTGCAAAA GTAATAAATC TGCTCTAAAG TCCCCTAATT AGATGAAAAA 720 AGAAGCCTGG TGCAGCTGAT CTGTGTGGAG ATGCACGACT TTATACCTTT TAAGTCCAGA 780 GGCCTGAGTG ACAAGAGCAG GAAAGGGAGG GAAACTGGTT GTCTGAGAAC GTTTTATGGG 840 CCAGCTAAAA CATAAAAGAG GTCACTGGCA TCAAGTGCTT GCTTTGCACA TAAAATACAC 900 AGTACGGTTG TTGCCCACAT GTTTGATAAA ACGTGGCTAT TCACTAACTT GGATTTTTTC 960 CAAATTAAAT TTCTGAATTC AGAATTAGCA ACCCTGAGCA ATGTAGAAAG CGATAAACTC 1020 CTTTTTAATG ACAAAAGTCA TCTGAACCTT AAGTGTCCAG TGCAACCTGA AGTGCTGCTA 1080 GTACTGTGGA TAGTCCGACT GGGCATGGGG AGGGGGTCTC TGGTTTTGGC TCTGGCATCT 1140 GCAGAGGCCG CCCCGTCTAA GCACACCCAT GACTGCTCTC TCCTGCTTGC GTCTTTGAGA 1200 AGAAGACAGT TCAGTCCCCC ACCACTGATT GTTTTCTGAC ACAGAGTTGA GTGGTTCAGT 1260 TGCTTTCTAC TTTTTGACTA ACAGAAGCCT GCGTCACTTT ACGTATTCTT CCTGGAAGCT 1320 CAGGCCCCAT GGTGTGTCTC TCTCACTGTC TCTCTCTCTC ACTGACTCTG TCAGTGACTC 1380 TCTCACTGAG TCATTGCGAC TCCCAGGAGC GTGACTATAG CTGTGACTTA TGGGTGTTGT 1440 GCAGTGTGTG GGGAAGCTGC TAGTGAGGTC GAGTTTAGCA GGAAGAGAAA ACAGGAATAG 1500 TGACTCACAC GGAGTAGTGG GGGCTGGGCA GATGAGAGAG TTAGGCAGCC CCGCCCTCTG 1560 CTGAGACTGG GACGCAGCCC AGATTCTGCA ACAGTGGGCA GAGGATTTGG CGATGGAGGC 1620 TAACAGGCAG CCAGGGGTCC TTTTTTTCTT TATTTTTATT TTGCTTAATT CAGAAAAGTA 1680 TGTGTGCATT TTGTGATGAA ATTCTCTACA GCTCTGTCTA CGAGAACTGC CCTGTAATAT 1740 CTCTGTGTGT TGGCTTTAAC AGTGAGCTAC TGATGAGATT CTGAGATTAG TCCCAGATCT 1800 TGTTTATGTC CTTGTTCCCC TTGAGGATAT TTTCTGAGTT AAATCAGGAA ATACCGATTA 1860 ATGGATGAAA ATGAGAAAGA GAGAAATAAT GTCCTTCGTA GGATAAGTCA TTTACCCTGA 1920 CTAGGTTAGC TAAGCTGTAT CACTCAATTA ATAATTAGGT GTGCATGACT CACCATTTTA 1980 GAAGGAGCCA TTGACAGCCC TAGCTGAAGT CAGCAAGTTC TGTATCTTCT CTAGCAAGCC 2040 ACTGGAGCTT TACAAATTCT CCTGGCAGGG GTGCATGTGT GTACGAGGAT GGAAGGGTCT 2100 GTGCACGGAT CTCCTAGAGA GATTTGAAAA TGCCTCGCCT TACTCCAGAT AGGTCTTTGG 2160 AGAATGTGCA TGTAGGATAG AATGGCTAAA ACGAAGACAA GCCAAACAGT TAGAGTGATC 2220
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