Tag | Content |
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EnhancerAtlas ID | HS088-03688 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:153656300-153657430 |
Target genes | Number: 24 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:153656852-153656873 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | Nr2f6(var.2) | MA0728.1 | chr1:153657086-153657101 | CGATCTCTTGACCTC | - | 6 | ZNF263 | MA0528.1 | chr1:153656779-153656800 | CAAGGAGGGAGGGGAGAAAAA | + | 6.09 | ZNF263 | MA0528.1 | chr1:153656451-153656472 | AGAGGAGAAAGAAAGAGAAGG | + | 6.21 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00751 | chr1:153655073-153656909 | Adipose_Nuclei | SE_02172 | chr1:153655647-153656913 | Aorta | SE_02172 | chr1:153657053-153658952 | Aorta |
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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: 2 | ID | Chromosome | Start | End |
GH01I153682 | chr1 | 153655074 | 153656913 | GH01I153684 | chr1 | 153657054 | 153662295 |
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Enhancer Sequence | GTGAGCTGTG ATGTGGGGGG TTGAGTGAGG CTGGGGGACC CGGAGAACCA ATAGCAGAGG 60 AGGCGGTGGG GACCCAGAGG GAAGAGGGCA GGGGTGAAGG GGCACCAGGG GAAAACCAAG 120 GGAGATGAGG AAGAAAGGAG GCTTAAAAGC CAGAGGAGAA AGAAAGAGAA GGGAATGGCA 180 GGGCGAGGGG AGGAGACAAG GATAGGAATG GCCAAGGAGA GTCAGAAAGA TCCAAGAAGC 240 AGAGAAGTTG ATGGGTGACA TCATAGGGGC GTGGACTGGT TTTCCTTGCT ACTCTTGCAG 300 GCCAGATAGG AAGCAACTTT CTGAACCTTT GCAATCATGC CCATGTTAGC TGAGGAGGGT 360 GAGCCCTGGT GTGTGCCAGG TGCCCAACCT AGAATGGAGA AGGGAGCTGA ATGAGCCTTG 420 TTCCTGCCGT CCAGTGGAGG CTAAAATGAA GTACAGGAGG AGTTAATGAT ATACAAAAGC 480 AAGGAGGGAG GGGAGAAAAA TCACTGCTGG TTGAGCATAT AATGTGTGCC AGGCACTTCC 540 ACGTACACTA TTTCTTTCTT TCTTTTTTTT TTTTTTTTTT TTTTTTGAGA CGGAGTCTCG 600 CTCTGTTGCC AGACTGGAGT GCAGTGGCAT GATCTAGGCT CACTGCAACC TCCGCCTCCC 660 AGTTTCAAGC AATTCTCCTG CCTCAGCCTC CCATGTAGCT GGGACTACAG GCACATGCCA 720 CCACGCTCAG CTAATTTTTG TATTTTTAGT AGAGACAGGG TTTCACCATG TTGGCCAGGA 780 TGGTCTCGAT CTCTTGACCT CATGATCCAC CCACCTTGGC CTCCCAAAGT GCTGGGATTA 840 CAGGCATGAG CCACTGTGCC TGGCCTCATG TTCACTATTT CTTTTCATTC TTATAATAGT 900 TAAGAATGAA ATAGATATTG CGGCCTCATT CCCAAGTAAG GACATTGAGG TGATTCCCCC 960 AAGGTCCCCA GTAAGGCAGA ATTTCCCCCA GCCATCCTGA TTCTCAGTCC AGAGGATAGA 1020 ATTCCCCCTC CATCTCTGAG TGCATGGTGT GGTCCCACGG CTCTGAGGAG GGGCTGCTGA 1080 GCACCCTGCC CTGGGTCAGC GGCTCAGCCA CAGGCTCAGA TGCAGCCTTC 1130
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