| Tag | Content |
|---|
EnhancerAtlas ID | HS108-02774 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:146745120-146746490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr1:146746067-146746077 | TTTAATTAGA | - | 6.02 | | CTCF | MA0139.1 | chr1:146745561-146745580 | TTGCCACCAGATGGCAGTG | + | 7.76 | | Klf1 | MA0493.1 | chr1:146745612-146745623 | TGGGTGTGGCT | - | 6.14 |
|
| | 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 |
| GH01I147272 | chr1 | 146744459 | 146747127 |
|
Enhancer Sequence | TTATCTCCCT AATAAAATTA ATAACATAAG ATTCATTTGG CCTCACTCTT CCAAGATCAT 60
AGACTGCACA TGGAGTCTCA GCCATTTTCT CATGTGATCA GTTGCCTCAG GGTTAGTCTC 120
AGGAGAAACT GAAAGAATCA GGCAGTGCAT CATCACTGCC GGGAAAACAG TTTTATTTAT 180
GCTTTAATGA TTTCATCATC CTCATATTCA GAGAGCAGCA TTATGTTTGA AATGTCTAAA 240
ATTAGGAAAA AAGAGATCTC TGCTTTTCAG TTAATCTCCT TGGAGGACTC AGAGTAGATC 300
TGGGAGCTGA AGCAGTCCTG GACATTAGTC TTCTCCAAAC ACTGTTGTGT TTGCTGTCAC 360
AGTTTTGTTG TAGTTTTGCA GTATTTTCAT TTATTTAACA GGTTTCCTTC CAAATTTCAA 420
ATATTTCTGT GATGAGTCAT GTTGCCACCA GATGGCAGTG ATAGCTCATG AATATGTTCC 480
TATTCATGGA TGTGGGTGTG GCTTATTTAT AAAAATCTCA CCCCTCGGTG AAGAGCTGCA 540
CTTAGACAAC ATGAATTCAA GAAGATAATT TTATGGAACA CATTTTAAAA TGAAATAAGC 600
ACCTGAAAAG TATTATAGTA TAGTGGATAA AAGCACGGGC TCTGGACCAA GACTGCAAGG 660
GAATGAATCC TGGCTCTTTC ACCTTCTAGG CTTGCAACTT CAGAGAAGTC CCTTACCCTC 720
CCTTTCAACA TCTATAAAGT GGGGAAAATC GTAGCAACTA CTCAACTTCC CGACAGGGTT 780
GTTGTGAGGG TTAAAGGAGT TAATATAGAG AGAGTGCTTA GAATAATGCC TGGCAAGTAG 840
TAAGCACAGC GTAAGTGTCA TTATCATTAT TATTAGGTAT AATTTAGCAT CTCTCAGTAA 900
TCGGTCATGA TTACCTCCTT GTTCCAACTT CAACTTGATA CGAAGACTTT AATTAGAATA 960
TTCCTGCCTG ATTTGTCTGG AGATCCAGCT TATGGTCAGT AGTCCTTCTT AAAAGTTAGT 1020
CCTTAATTCA GGTTTATGGA ACAAGCCCTT TCAGGCTTGC TTGTTTCAGC AACCAGCTCT 1080
AACGACCCTG GCAAGAGGGA GTCTGTTTTG TACTTGTTTT CACATTAATC AAAGAGAAGG 1140
CTGCAATGTA CCTTCACGGT TCTCTTAATT AATTCCTGTA ACTCAAGGTA CCTCCTCAGC 1200
TCTCTTCCTG CAGCACTGAA GAAAGACCAG CAAGAGTGTT CTGAGCAAGC CTCAGAACAC 1260
TCAGAGTAAA TGACAAGAGT GTTCTTGTCT TGCCGTTGGT TTTGTTACTT TCTTTTTGAT 1320
TAATGTGGAA ACCAGTACAA AAAAGACTCA CTGGAGTTTT CTCTAATCAG 1370
|
