Tag | Content |
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EnhancerAtlas ID | HS112-00269 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr1:35383930-35385340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZEB1 | MA0103.3 | chr1:35384639-35384650 | GGGCAGGTGGG | - | 6.14 | ZNF263 | MA0528.1 | chr1:35384570-35384591 | GCCTCCTCTCCTCTCTTCTCC | - | 6 | ZNF263 | MA0528.1 | chr1:35384576-35384597 | TCTCCTCTCTTCTCCTCCCTT | - | 6 | ZNF263 | MA0528.1 | chr1:35384573-35384594 | TCCTCTCCTCTCTTCTCCTCC | - | 7.42 |
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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 |
GH01I034918 | chr1 | 35384360 | 35385201 |
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Enhancer Sequence | GCAGGACCCT TACAGTGCCC AGGGTGGAGG CAGACAAGGG GGTCTGCTCA ATGCGGAGCT 60 GATGTGGTCT CAGCCAGGCC TTGGCCCACC CCTGCCTCAC TGAGAACAGA CTCAGCCTGG 120 TGCAGATGGC AGGGGAGGAC CCCTCCACAC AGGTTCACCT GCTACCCTTA GGAAGTGGGT 180 CCAGCACGTG GCTAATAGGC TGAGGATGGG GCAGAGGCCC GGGCAGGGGG GCTCAGGAAA 240 TCAGCCGGGG AACAGGCCCC AGTCCGATTG GCTGAAAAGT GGGTCATTTT CCTTTTGAAA 300 AATAGTGAGA AAATGGAGAA GTAGGTCGGG CTCTTATCCC CTCAGCCCCA GGCACCATCC 360 CCGACTTGAG GGGTAAGGAG AGAGGGAGAC GCCTGAGCAT GCCAAAGCCC CATATACCCT 420 AGGACCCTGG CCAGGGCCCC ACAGTGCAGG AAGCCAAGGT CATCATTACT CAGGACATCC 480 AAGGACATGC ACACTCCGAG GCCAGAGCTG GAACACCAGC CCCACCCTGC CCCAGGGGAT 540 CTGGGGTGAA AGGAGCTAGG GCCGGGGCCA AGCTAGAGGG GTGGGGGCTT CCACCCGCAG 600 GACCCTGAAG AGCCCCTCCC ATCCTCGTGT CTGCTGTGAT GCCTCCTCTC CTCTCTTCTC 660 CTCCCTTTCC TCATCGTCCA CGTGGGCAGA GTCGTTGCCA TGACACCGCG GGCAGGTGGG 720 CGGCTCTGGC GGCTGTTTCG GCCCAACCCC CATGCTCACA GCCCAGGTGG GAGGGGAGCG 780 GCTGCAGCAC CCTGGCCCCT AGCCCAGATG AGAGAGGAGA GAGGCAAGAG GCCCCCCTTC 840 ACCCCTAGAG CCTGGAAGGG GCTCTATCAC TGGCCTCTCG ACCCAGCCCC ATGCTTGCAG 900 GTCCGGGGGA GGAAGTGTCA AAGAGGATCT TAGGCCTTGA CCACTCCCCT CCACCAGAGG 960 TCCCTGGAGT GGCATGGGGT GGGGCAGACC CCCAACTCCC ACTTCCTCCT TTTCTTAGCA 1020 GCTGTCCTCC CAGCTTTCCC CACATACTAT GCCTTAGTCT CTTAATGCTA GCAGCTGATT 1080 GGTCCTGCCT GAGGTTTAAC CTCAGTTGCT CATTTTGCAA CACAAGCTCA ATTCTCCATG 1140 CTCTCTTGGG AGAAAGGAAA ACAACCAGGC CGGGTGCAGT GACTCATACC TGTAATCCCA 1200 GCACTTTGGG AGGCCGAGGT GGGCGGATCA CTTGAGGTCA GGAGTTCGAG ACCAGCCTGG 1260 CCAACATGGT GAAATCCCCA TATCTACTAA AAATACAAAA ATTAGTCGGG CGTGGTGGCA 1320 AGTGCCTGTA ATCCCAGCTA CTCAGGAGGC TGAGACAGGG GAATCGCTTG AAAGCAGGAG 1380 GCAGAGGTTG CAGTAAGCTG AGATCATGCC 1410
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