Tag | Content |
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EnhancerAtlas ID | HS133-08812 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr13:99195590-99196970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr13:99196451-99196466 | TGACCTCTGCCCCAG | - | 6.06 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_18352 | chr13:99191700-99197126 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19168 | chr13:99193411-99197373 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23248 | chr13:99195572-99196281 | Colon_Crypt_1 | SE_23248 | chr13:99196301-99196992 | Colon_Crypt_1 | SE_27798 | chr13:99192233-99197145 | Fetal_Intestine | SE_28780 | chr13:99195763-99197012 | Fetal_Intestine_Large | SE_45616 | chr13:99191234-99197022 | Osteoblasts | SE_52580 | chr13:99191942-99197052 | Small_Intestine |
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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 |
GH13I098539 | chr13 | 99191481 | 99196993 |
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Enhancer Sequence | AGATTTGAGA AACCTCGACC CTCCAGAAGC ACCAAGCAAA AAAGGTCTCC AAGCACAAAC 60 ACAGCTGCCC CAAATTCCCG GTCTGCCCAA ACTGCACCTC TCAGAGTGGG GCCTCAGTCC 120 TGCTCTCAGA ACATTCTGGT GCGTAATAAA GGCACACACT ACGAAAGGTC AAACAGCTGG 180 TCTCCATCAA CAGCAGCTGA GAAGCAGCAG GTGAGGCCAG GGTGGGCGCG GACCCGAAGA 240 CGCGGGTCTG ATCGCTGCAG AGAGACAGAG AATACAGAGA GAGGGGAGGC AGCAACAGGA 300 GACCCCGCAC TGGGGCCCGG AAGCCCTCTA CTCCCAAGTG GCCCCCAAGG ATGGTGCTGA 360 ACTATGGTAG GACGCAGGAC ACCCCTCGAC TGCAAGAGAG GAGCTGCCAG CCGCCCCGAG 420 GGTGAAGCCT GCAGATGCGG TGCCGGTCAT CAATGGCTTC TATTGAACGG ATCACCGCCA 480 GAAGCTGCCA TCCACGACTC AGTATCCGGC AGACTCGGTC ACCCACACGC ATAAACCACA 540 TGCTATACAA AAGAAACTTG ATTTTACTTC TGGGTCTTTT TTGATCCTAG GCTTCATAAG 600 AACAGCACAC AATGTAAATT GGCAAGTGTG AGTATCCTGG CTCTAATTTG GAGTCATGTT 660 AGTGGACCTC AGGTTTAAAA ATAGCTATGA AGAGGCTTCT AGTAAAAGCC ATTAAATGAA 720 AGGTGCATTT ACGTTAGGCT GCTGTGGCCC ACGCTGAAGT TAATAAAGGA AGGAGAGTGA 780 GAAGAAAAGT CCATCTGCAA TAAAACTAGG AACTACTCTC ACCTGAACCC ACAGATGACA 840 AAGACTACCT GCCGGGCACA ATGACCTCTG CCCCAGGCTG AGGCGACAAC TGAGAACACA 900 GCAGGACCTT AGGCCAGCAC AGGGGCAGGA GGCTCTGAAA CTGAGGTGGC AGGTACGTTC 960 CCGTGGCCCA ACTGCAGACA CAGAAGTCCC CAGCAGGCCT GGCCCACGAG GGCATCTCCA 1020 CTTCCCTAAC CAGGAAGGTT TCCTGGAAGA GAGGCCAGCT TTGCACTGTG GGCCCCAGGC 1080 AACTGGGCCC TGACCCTGCA TCTGGGAAGC AAGGGCCCTA CTGGGAGTGG CGCAGCCCCC 1140 CTGGAGTATC TCATCCCGCC GGGTAGAGCA GGCAGAGGCA CAGCCAGCCG GCAGAAGGCA 1200 GGGCAGGCCG GAGAGGAGAG GACAGAGCCG CCCGCCCCAG GAGGCAATGC TCCCCACCCT 1260 CCAAGCCGAC CTGAGGCCAG GGTACATGGC AGGTCCCCTC CTAAGCCAAA GAATCCACAC 1320 CGAGGCATGC GGAGACGCCT CTACAAGGAA AGACAGTGGT GAAAAAGAAA ACAAGCAAAA 1380
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