| Tag | Content |
|---|
EnhancerAtlas ID | HS052-02997 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:181998450-181999580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:181999215-181999234 | CGCCGCCCCCTTGTGGTCT | - | 6.79 | | KLF16 | MA0741.1 | chr1:181998920-181998931 | GGGGGCGGGGC | - | 6.02 | | KLF16 | MA0741.1 | chr1:181999118-181999129 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr1:181998921-181998931 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr1:181999119-181999129 | GGGGCGGGGC | - | 6.02 | | SP1 | MA0079.4 | chr1:181998919-181998934 | AGGGGGCGGGGCCTG | - | 6.75 | | SP2 | MA0516.2 | chr1:181998918-181998935 | CAGGGGGCGGGGCCTGG | - | 6.27 | | SP3 | MA0746.2 | chr1:181999117-181999130 | GGGGGGCGGGGCG | - | 6.11 | | SP4 | MA0685.1 | chr1:181998917-181998934 | ACAGGGGGCGGGGCCTG | - | 6.88 | | Zfx | MA0146.2 | chr1:181998920-181998934 | GGGGGCGGGGCCTG | + | 6.19 |
|
| | 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 |
| GH01I182028 | chr1 | 181997913 | 181999747 |
|
Enhancer Sequence | ACCTATGGTG ATCCTCTCAC CGAGGCCTGC TATTTTCTCT TACTGGAACT CTGTCCCCTC 60
CCCTGGGCAC CCTCCCGCCT CTGGCCTAGC GAATTCCTTC CATCTTCCGG TCTCAGTTCC 120
TCCAAGAAAC CTTCTCACCT AACCCGTCCG GTCAGGGTAC TTTCCTTACC TAACACCCAC 180
TCCCTCGTTT ACTTCTCTTT GGCTGGACTG AAGTTGGGCA GGGCAGGGGC TAGTCTGCCT 240
TCTTCTGGGC CCAACCCTCC CGGCCGGCAC CACAGGCATT ACAGGTACTC TGTGCACTCA 300
GGCTGCGCAG ACCCGCAGCT TCCTATCCTG TAGCTCACTT TCCTCTGAGG CGGGCTGGAG 360
GCGGAGCTTG TCCGCTGGGG GTGGGGCTCA AAGCTGGGGC GGGGATACGG AGCAAAACTT 420
AAGAGGAAGA TGAGAAGCCT GGTTGGCCAG GAGGCTTATC TGTCAGGACA GGGGGCGGGG 480
CCTGGGGGGC CGTACCTTTG CTTACCGCGA GTGGGCGGGG CAGGTTTTAC CGCCGCGGCC 540
CATCAGCGAA GATCGCTGAG CGGCGCCCGC CTTGCGGGCC TCCAGGACCC GGCCGCCGCC 600
ATCCGGTGGG AAGCCGGGTG GCCTGCGGGT GAGGGGGGCG AGGCGGACGG AGGGCACCAC 660
ACCCCCCGGG GGGCGGGGCG GGCGGAGAGC ACCCTACATC CGGGAGCCGG GGCGGCGCCT 720
GGAGAGCGGA GCAGGCAGCG CTTTCTGCCC GCTGAGTGGG TCAGGCGCCG CCCCCTTGTG 780
GTCTCGGCCT GCGGGCAGCC CTTTGGAGCG CGCGGGAACC GGACGCCCGC CCGAGGAGAG 840
AGGATCCAGG AGACCACTCC GGGCGGGATC CGCGGAGCCT GGGGCCGGGC GGTTGGCCCA 900
CATTATAAGA GGGCCTGCGT TGCTTCTACC TCAAAGGCTT TAGGGTGTTT GTTAATTCCC 960
CGCCCCCCAA CCTGATGATG CTCCAGGTAT TTACAGGCAG GTGCCCCATA GGCTGTTTAC 1020
TGGGAAGCAG AATTGGTGGA CTCCGTTCGG GGATATGAGG AAAGATCCAT AAGCAGAGAG 1080
AATAAAGCCT TTGCACTTAC ATTTTACTTC TCTTATCCCT CACCTCTACC 1130
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