Tag | Content |
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EnhancerAtlas ID | HS138-25772 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr22:46910250-46911690 |
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) |
MITF | MA0620.2 | chr22:46911265-46911283 | CCAAGTCACATGACCCCC | + | 6.01 | MITF | MA0620.2 | chr22:46911265-46911283 | CCAAGTCACATGACCCCC | - | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26636 | chr22:46909700-46911877 | Esophagus | SE_34191 | chr22:46909995-46911887 | HCC1954 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH22I046513 | chr22 | 46909817 | 46911837 |
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Enhancer Sequence | TATGTGATGC TGAAGCTCTT CCACCCAGAC GTTTCACCAG GCCCCGACGG TCCATCCAGG 60 TGAGGGCTGG AGTCAGGTCC ACCTGCACTC TGATCCCCGG GGGCCCAAGG CCACACACCT 120 CTGGCTGCCA GTCAGTCAGA ACCAGTCCTG GTGAGGTGGG GAGTGGGGGC ATGAAGGATG 180 TGGCCTGAGG ACACCCCAAC AGCATCTGTG TATCACCGCC AGACCCTTGC TGAAAGTCAG 240 GGATAATGCA ATGGCCCCTC TCAGCACCTC CCCAGACCTC CCCAGACTCT GTGGTCCCTC 300 CTCCCAGCAT CAAAGAGAAG AGTCACTCCC CGGAGGGAGC CGGGGCTGCA GGGCCGAGGC 360 TCACGGCTGG GCTCTGGAAT AAGAGGGGTG TTTCTGAATG AATTGCCCAG CCCTGTCCTG 420 CCTCGCTGAG TCATTCCCAA GTCAGCAAGC ACAAGTCACT GCGGGAAAAG CTCTGGAGCT 480 GCCACCCCTT CCCACCCCAG GGATGCCTGT CCGTACCCGC CGTCAATCCA GCCCTCAGGC 540 CTGGGGGATG AGCACCTCAG ACGTGCTCTT TGCAGCTGGC ATCCGCTCCA AACTCCATGC 600 CTCCCCACAA AAGTGGCTCT GTCCAAACCC CAGCCCTCTT GGGCCCTGGC AACCAGCCTA 660 GTCCTCGCCA GCCCCTTCTA GAAAGCACCC CCAGCACCCC CTCAGCTTCA GCCTGGGCTG 720 AGAAAAGGCT GTCTGGCAGC GTGGACCCCC CTCAGCGTCC CAGCAGAGCC AACCCCCCCC 780 GGGGACACTC ATGGGACACA GCATGGGCAG TAGGAGCCAT TCCACCCGTG CATCAGCCCT 840 CTGGCCACAC TCTGGGACCT CATGGCCCTG CCCACCACTC CCAGCCCACA GCCAGGCAAG 900 TGACCCCCAC CTGGGCCCTC CTGGGGAGAG CTGCACAGCT GTCGGCAGCA CAGCTGGAAC 960 CACAGCCCAG CGGTCTCAGT GCGTATCACA AAGGCTAGCT TGTGAGTGGA TGCTCCCAAG 1020 TCACATGACC CCCAGGTAGG AAGGTTTGCA CATGTTTCAT CAGGGTAAAG GGAAAGAGGC 1080 TCACCTTAAA CACAAACTCT ATGAAGGCCT TAGACAGAAA ATAGGAAAGC ATGACAGTCT 1140 GTGTCTCCAT GGTGAAGTCA GCTCTGGGAG GGCTGAGCCT GATGCAGAGT GGGTGTGCAC 1200 AAGCTGCAGG GCACCCCGGG GGCTGGAGGT GGAGGACACA GCCAATAGGA CGGGCCTCAG 1260 TCACACAGTG CTCAGGGCTG GGGACTCAAA GGCACAGAGG CTGAGGCTTT GTAAGTCCTG 1320 CTGGGGGATC AGGGGATGAC TAAGTCACTG GGGCCTCCCC AGCCTGGCAG GCTCCTATCT 1380 GTGTAACAGG CTCCCAGCAG CCAGTGTAGG AAGGCAGCCC CGGCAGGAGG ATACACCAGG 1440
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