Tag | Content |
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EnhancerAtlas ID | HS147-27401 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr22:43559250-43561220 |
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) |
SPI1 | MA0080.4 | chr22:43560091-43560105 | TGCTTCCTCTTTTC | - | 6 | SPIC | MA0687.1 | chr22:43560091-43560105 | TGCTTCCTCTTTTC | - | 6.1 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_23668 | chr22:43559512-43560072 | Colon_Crypt_1 | SE_24969 | chr22:43558628-43560231 | Colon_Crypt_3 | SE_26727 | chr22:43558596-43561245 | Esophagus | SE_32000 | chr22:43558390-43560967 | Gastric |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr22 | 43560000 | 43560338 | chr22 | 43559294 | 43559513 | chr22 | 43559631 | 43560203 | chr22 | 43561104 | 43561179 | chr22 | 43560240 | 43561090 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I043163 | chr22 | 43559100 | 43560546 |
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Enhancer Sequence | ATGGCCTTTT TGCTTGGGTG GGACCCCTGG CCACAGGGAA GAGGGGGAGC TGGGGCTGCA 60 CTGGAGCTCG TCTCTGCAGG ATCTGCCTGG GCTGCCTTCT CCAGACAGGG CTGGATCCAG 120 CTGGGGCTGC CCCACGCTTC CTGGGACGCT CCCGAAGCCC TGCAGGAGAT GAACAGAGCA 180 GCCCTGGGTG CCACCCTGGG GCCCACACTG GCGCAGACCC AGCTGGGGCC GTGGGCTTCA 240 GCAGAGGGAG GGGGTCCTGT CCGCTTCCCA TGGCTTCCGG GATGCTCAGC CCGGGCCCTT 300 TAATGGCCGG GCCCACAACC ACTGTTCGAC GCCTGGTCCT GCCCAGTGCG TGGCCCTCAG 360 CTGCTTTTAC CCAGGACAGA GTTGGGGGTG CTGACTGCCC TGTCCCCCGG GGGCCCAGGC 420 TTATGGCAGC CTCACTGCAC CAGGGATAGC CCCGCAAACA CCCAGTTGGC TCGAGGGGGA 480 GTCAGAGGCA GGAAAGGTTA GGTCCCGACT CCAGCAGACA GGGCCTCCTT GCTGGCCCAG 540 AGCGGCCAGG ATTGGAGGTG TCACAGCCAC TCACTCCCTC ACCCCGGCTT CGAACTGGGT 600 GACCCATGGC CTCTCCAGGC AGCTGTTTGG AGTAAATGAG CCGAGTCCCA TACGCAGCAC 660 TCCTCCGTCT TGCTCTCGGT CACCACACCC ATGCAGCACT CAGCAACACA GCCCGCGGCT 720 CCCTCCCCTC GGCCAGGCCT GACCTGCCGG GCTTTTTGTT TTTTGTTTTT GGCAGCTAAG 780 TTCATTCAAA TTGGCAAAAT GTTCATAGAC AGCTCGTCAT CACTCAACAG CCCGCGGCTG 840 CTGCTTCCTC TTTTCTCCCC CGGCTCCTGT GTCCTCTCCC GACCTGTACG CTCAGACACA 900 ACCTGACGTT CACAAAAGCT TGGACACAGT GGCTCACACC TGTAATCCCA GCACTTTGGG 960 AGGCTGAGGC GGGAGGATTG CTTGAGGCCA GGTGTTTGAG ACCAGCCTGG GCAACATAGG 1020 GAGACTCTTG TCTATACCAT CCACTCTGGT GCACGCACAA CACACACACA CACACACACA 1080 CACACACACA CACACACGAA AGAACGAACA GCTCAGGGAA ATGGGTAGAC AGTCGACTGC 1140 ATTCTTCTGA CAGAAGGGAT GGCTCCCGCC CAGGGGCTGC GCTACTCCAC CCTGACCCTC 1200 AGCCTCCCGC TCCCTTGACT CTGGCAGAGT TTGATGCCCA ACAGATCACG CTCTGCAGGA 1260 TCCAAAAACT CTGCGGCCAC GGGCACTCAG CTGAGCCCTC AGCCCTCATG GCTTTCCCGA 1320 TGCTCACCGG TGCAGAGGAG CCAGCTGGGG AGCCTCTGTG TATCCTTTTT ATTAACTTAT 1380 TTCTGAAGTT CTCCAAGACG CCCAGAGTTG AATTCCTCCA GAGCTCTGTG CAGACAGTCC 1440 AAGCAGCGGA TGGCAGAGAG GTCCTTGCTA GCAAGAAACT TACAGGCCAG GCTGTCTCCT 1500 GCTCCAGCAT GCCGGTGAGC ATGCACCGTC CCCGCAGGGC ACAGGGGTAT CCTTTGAAGT 1560 GTCAAGGGAC ACCTGAGTCC GTGCCAGACA CTTAGGGATT GGAGAAAGTG CAACCCAGAC 1620 TTCTGCCATC TCCGCAACTC GTGGGGTTGT TCATCTGTAA CAAATGTCCC ACATAGCTCC 1680 TGCTGGCCAC AAAACACGCA CTGCCACAAA ACGCCTTGGA AAAATGGGCG AGAGGAGAAC 1740 GCATTTAGCA TTTCGTCTGC CGGCTTCCTT TTAACAGCCT GGCGACGTTT CCCCAGGAAA 1800 TGCTCGTAAC AGACAGCATT CTCTCCTTTT CTAAGCTGCT GTCATCCACT GGGAACTTAA 1860 GGTTTTGATG CTTTCTGAGT GGGTTTATTT ATTATTTTTT TTTGAGACAG TCTTGCTCTA 1920 TCGCCCAGGC TGGAGTGCAG TGACGCCATC TTGGCTCACT GCAACCTCTG 1970
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