Tag | Content |
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EnhancerAtlas ID | HS105-29578 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr16:3690340-3691240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr16:3691160-3691174 | TGGGGGGCGTGGCC | - | 6.83 | KLF16 | MA0741.1 | chr16:3691162-3691173 | GGGGGCGTGGC | - | 6.62 | SP3 | MA0746.2 | chr16:3691161-3691174 | GGGGGGCGTGGCC | - | 7.22 | SP8 | MA0747.1 | chr16:3691161-3691173 | GGGGGGCGTGGC | - | 6.44 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27804 | chr16:3686820-3694007 | Fetal_Intestine | SE_28680 | chr16:3686810-3694100 | Fetal_Intestine_Large |
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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 |
GH16I003636 | chr16 | 3686905 | 3693735 |
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Enhancer Sequence | TAGCAGCAGC CTTGGCCTCC CTGAGCTCTG AACTCTGTCT TCCCAACTCA GAAAGACTGC 60 AGGTTCCGGC TGAGTTTCCC TGCCTGCGCT GCAGCCTGGA ACCCGCCTCC TGGCTGTAAT 120 TGGTGCAGTC ATAGGATGTG CTCTCTTGTC TCCCTTATCT TGGAATCACT GTCCTGCACT 180 GTTTTCCACC AACTGAAGGC AAAAGTATGT TGTCCAGTTT TCCAGGTGTT CAGGGTTCCC 240 TGTTGCTGCA TCCTACATGA GTATATAAAC AGAGAACAAA CAAAACAGCC TGTCAGGAGT 300 TTGCTGAAGT TTCAGAATAG GTGGTGCTGG GTGAGCTGAT GGGCATGAGT AACACTCCCC 360 TTTTCCTTCT TTTAGTGACC ACAATATGAA TGGGAACAGC AAGATGGCAA AAGCTTGCTG 420 AGTGGTACAG CGCCAGCCTG GGTAGTGGCC TCCCCAGCAA GTTGCATGTC ACTAGCTTCC 480 TGTGGCTGTC ACTCCTGGGC CCAGGCACCT CCGAAGATCA GCACCTCCTC ATGGGCTCAA 540 GCGAGGACAG GAGCCCGTCA CCCATGAGCT CTCAAGGGCA GAGCCACTGT CCTGTCTCGA 600 TGGCTCCACC GTGACTCCAG TGGACTTTGG ACAGTGGGGA GCAGGCCCAA CAGGGCCACT 660 CGGATGTGGT CACTCTGGAT TTGGGTGGAT CAGCACCAAG CTAGACTCAT CCCCAGCCCC 720 CAGGTGCTGT TGCTGCTCCT GCGTGAGGCC CCATCCACAG CTGCAGCTGT GGCAGGGTGG 780 CTAGTGGTGG CCAGCATGGC CCTGCTGCAG CTCCACGCTG TGGGGGGCGT GGCCCTGACC 840 AGCAGCCACC CCTCCATGTG GGCCACAGGG GAGGAGCTTA GGAAGCCGCC TTGGCAAGGT 900
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