Tag | Content |
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EnhancerAtlas ID | HS060-28848 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:484120-485130 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr6:484646-484657 | GAGCCATAAAA | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_18670 | chr6:483771-485538 | CD4p_CD25-_Il17-_PMAstim_Th | SE_58878 | chr6:468375-503300 | Ly3 | SE_61068 | chr6:422752-507076 | HBL1 |
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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 |
GH06I000483 | chr6 | 483772 | 485538 |
|
Enhancer Sequence | TTTAAAAAAA TCTACATGCA AAGATGACAA GAGACAGGAG AATGAGTCAG TGTGCTCAGC 60 CTAAGGCAAT GATGCTTGTT TTGCAATGCC CAAATCATTT CTAGAATATG CTCTTTCATG 120 GTACACTGAT AAAGAAAGTC TTAGTAAAAA ACCAAGTGAT TTCTAATAGC TCTTTCCCAT 180 TCAAGTGAGG CCAGCTCAGC TAACTCACAT GAAGCCATGC TGTGACCCAC AAAGAACATG 240 GGTGTGCTGG AAATGAAATG CCACTGGAGC ACTGAAGTAC CTTGAACCTC CCTAATTTGT 300 TTTCTCAGCT GCCTCGTTAA CTTGCTCCAG GTCCTGGTTT CTCTCTCGGC TTTCATCTAA 360 CTTATTTCAT ATTCATCTCC TCTTACCCAC TAAACCAGGG TTCTGTAACT CAAGTAGCTC 420 TTGAAATCCC CCTTTCTTCC AAGAAGTCCC CCCTGACTTG TTGGAATAGT AGTCCTTGAA 480 CTCCCTCACT TGGGTATGGG GTTTTTAGGC CTTTACCTTC CACTCTGAGC CATAAAAGCA 540 CTACCGGTTT CCGTGTTGCT ACTGTTTATT AGCCTCTGGA ATTGATGAAC TTTCTCTGAG 600 CTGTGACCCA GGTGGATGGA TGTCAGAAAG CATATTCCGC TGGAAGGAAG AGCTGAGCAG 660 TAGTGAAGTC AAGGACATAC AGAGCCAGAG TGTGAACATG AGTCCTGCTA CTTACTGCCT 720 TGCAGTCTTA CGGAAGTCAC CAACCTCTCT CTAAGCCCTG ATTCCTTCCT CTGCTAAATG 780 GACGTGGCGG TAAGCTAGCC CACATGTATC ATAAGGCTGT TGTGAGGATT CAACGAGGCA 840 CTTCATGGTG TGCCTCGCAC ATGGTAAGTC CCCAGCAAAC AGAATTAGCA GGACCTGACA 900 GATGGTTTCT GACAATGTGT TTACCAATAC AGGGTTAACC AGAATGTAAG TATTTTGGGT 960 GTTAACAGTA GAAATATGAA AATGTTGAAA TAAAGACACT TAGGGAAAAA 1010
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