Tag | Content |
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EnhancerAtlas ID | HS017-09497 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr14:22890940-22891930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Tcf12 | MA0521.1 | chr14:22891421-22891432 | AACAGCTGCTG | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_19974 | chr14:22885877-22892207 | CD56 |
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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 |
GH14I022421 | chr14 | 22890793 | 22892035 |
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Enhancer Sequence | GAGCTCAATA AAGATCAGGA AACTCTGGCT CACATTTGGA AGACCATGTT TCATTGGATT 60 GCTCTTTAAC ACATGGGTAA ATCACCCTTA TCCAACTTTG CCTAGAGGGA GTTTGCAGTG 120 AACACAACAA TCATTACAAC ATCTTCAGTC TTTGTGCACA TGCTATTGAT CTCCTCATTT 180 GGTGGTTCTT TTGATTACAG CTGTAAATGC CAATAATTCT TCTTGGTATG AACTATGAAC 240 ATCACCACAT AGTGTCTAAC ATGTACATCT AACCTGAAAC TGGAACAACA ATATCAAATT 300 TAACGTCTAG GGAAGGAAGC AGAAACCCTG TCACCAATTA AATAAGCTGC CTTAATCTCC 360 TCTCAGTTGG CCTAACTTAC CTGAACCGTA CTATTGGTCT TGAAGGTGGC ACTGTCATCC 420 CATTAGCAGG CAGCAGGCCC TGCGAGCCTC CTGTGATCAG CTAGATTTCT CTGGGGAATG 480 AAACAGCTGC TGATAGGGAC TGACTTCCTC AGTCACAAGT GTTTCACAAG TGTGTTGGTT 540 CAGAGGAGGG ACCAGGCAGA AGGTGGTTGA GAGGCAGAGC TGCCCCTGAG TGAGCCATGC 600 AGAGGATCTC CTCCCTCATC CATCTCTCTC TCTTCTGGGC AGGTAAGGCA GACCCCAGAA 660 CTTGGGCCAA GCAAGACTCA GCAGCAAAGA AACATCAAGG CTCACAGGAC CTTGTACTCA 720 TGGACTGTGC TCCTTACTCA ATGACCTCAG CCCCCAGCCC TCACTGAGCC CCTCTCTTGT 780 GTCTTTTCTC TCAGGAGTCA TGTCAGCCAT TGAGTTGGTG CCTGAACACC AAACAGTGCC 840 TGTGTCAATA GGGGTCCCTG CCACCCTCAG GTGCTCCATG AAAGGAGAAG CGATCGGTAA 900 CTACTATATC AACTGGTACA GGAAGACCCA AGGTAACACA ATGACTTTCA TATACCGAGA 960 AAAGGACATC TATGGCCCTG GTTTCAAAGA 990
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