Tag | Content |
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EnhancerAtlas ID | HS053-18885 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr19:1897380-1898150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr19:1897720-1897731 | CTTCTGGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr19:1897720-1897734 | CTTCTGGGAAAGGG | + | 6.38 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_16076 | chr19:1897369-1898070 | CD4_Naive_Primary_7pool | SE_16627 | chr19:1897264-1898280 | CD4_Naive_Primary_8pool | SE_17066 | chr19:1897361-1898081 | CD4p_CD225int_CD127p_Tmem | SE_18006 | chr19:1897111-1898511 | CD4p_CD25-_CD45ROp_Memory | SE_20207 | chr19:1895084-1898764 | CD56 | SE_20804 | chr19:1897129-1898577 | CD8_Memory_7pool | SE_21628 | chr19:1897187-1898228 | CD8_Naive_7pool | SE_22168 | chr19:1897343-1898194 | CD8_Naive_8pool | SE_22514 | chr19:1895087-1898475 | CD8_primiary |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 1897896 | 1898000 | chr19 | 1898000 | 1898017 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I001895 | chr19 | 1895000 | 1898669 |
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Enhancer Sequence | CTCAGGGTTC ACGCCATTCT CCTGCCTCAG CCCCCCGGAT AGCTGGATTA CAGGCGCCCA 60 CCACCACACC CGGCTAATTT TTTGTATATT TAGTAGAGAC GGGGTTTCAC CGTGTTAGCC 120 AGGGTGGTCT CGATCTCCTG ACCTCGTGAT CCACCTGCCT CGGCCTCCCA AAGTGCTGGG 180 ATTACAGGCG TGAGCCACCG CACCCGGGTG ACACTCCATT TTTGACCCCA GTGTTAGCAC 240 AGAGCTTTTA AACTTCCGCA CTGCTGATGA GGGAGTGTGA TTGTTCTCTG TTACCAGCAC 300 TGTCTCCCGC CCACCGGAGC CGAGTGTGGT GGGTGTGGAC CTTCTGGGAA AGGGTGTAAA 360 CACGTGCTTA GATCCGGCCG GAAGCCCCGT GACCGGGGTG CAGCTGCCTT TGGTCAGTAG 420 GTGGCAACCG TGTCCGCTTG ATTTTGGGAG GGTCCGAGAG GCTGGTGCAG GGCTCCCAGG 480 AGAGGCGGGG GCGATCCCAC TTGCCTTGCC AGGATAACAG CAACAAGGGC TGCCCACGTG 540 CATGCTGGGC AATAGGGATA CCGCAGAGAA TGAAAGTCCA GCCCTAGCAG GGCAGCAAGA 600 CCTCGACTCT ACAAAAATTT CAACCACAAC AAAAATTAGC TGGGCGTGAC GGAACACATC 660 TGTGGTCCCA GCTACATGGG AGGCTGAGGT GGGAGGATCG CTTGAGCCCG GGTGGCAAAG 720 GCCACAGTGA GCTATGACTG CACAACTGCA CTCCAGCCTG GGTGACAGAG 770
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