| Tag | Content |
|---|
EnhancerAtlas ID | HS108-02319 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:93498440-93499860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:93499505-93499526 | AGTTTCTTTCCCTTTCAGTTC | + | 6.29 | | NFE2L1 | MA0089.2 | chr1:93498750-93498765 | AAATGACTCAGCAAT | + | 8.07 | | Nfe2l2 | MA0150.2 | chr1:93498748-93498763 | CAAAATGACTCAGCA | + | 7.82 | | ZBTB18 | MA0698.1 | chr1:93498583-93498596 | GCACATCTGGATC | - | 6.41 |
|
| | 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 |
| GH01I093032 | chr1 | 93498529 | 93500070 |
|
Enhancer Sequence | GCAATATTTA TTATCGTTGA GCATTTGCAA TTTTAATTTA CAAACTACCT TTCTATCCAT 60
TTATTCTGAT GCTCTGCTGT GCTTCTTAGA GAGGGTTAGG AGGTTGAAGA GCTTTGTATC 120
AGACCTCTCT TGGTTTACCT GATGCACATC TGGATCAGAT GCATGCCCCG TTGAGCTACA 180
TGCATGCCCC ATGCTCCCAG CAACATCCAA CTGCTCAACC CCTCCCCTGT TCCCTGTCAA 240
CCACAGGCCC TCTTGGGGGT TAAAACCTTT TGAACAGGGC CATCTGTTCT TCACTTCGAC 300
AAGTTGAGCA AAATGACTCA GCAATTCACT CTTCTAGTTT TTTAAGTCAG GACAGGATAA 360
GGGAGAGATG AAAACATCCA ATTCAATTCC AAGAACTTGC CAAACAATAC GTCATTTGCT 420
CAAAGTCACT CAGTTGGGAA GAAAGATTAG AACTCAAGAA ATGTTATGCC CTCAGATGCA 480
CTGCTTATCC AAAAATGTAT CTAAAATGAT TTAGAAATCT CGTATTTCAA TCAGCGTTGG 540
CTTCACAGGT GTGCAACCTG TGCAATCACA CAGGGTCCAC TCTCAGAAGA GCTTTGCACT 600
TGGTTGAATG CTCTGCTGTC TCCATTTTGA AATTCTTAGT TATTTTACTT TTGAACTTAT 660
ATTTTGTAAG TGATGTTCAA TGGGACAATG GCATGAGCAG AGAAGATACA TGAGTGCCTT 720
CCAGTCTTTG TTACTAAATC TGTCTGCATA TGGCTCTCCA GATTTGCTCC ATGAACACAG 780
AATTCCACTA CAGACCCACA ATGCCTAGAA ATGTAGCAGA CACAAAGGAA GTACATGATT 840
AGCATGTATG TCCACAAATA AGTAGGCACT GACAGTCCTG AGAGGCCATG TTTTCCATTC 900
AAACCGGAGC CTGTTTTGAC TGCAGAGAGA AAGCAAAGGC ATCCTAAAAA AAATTATCAA 960
AGGAATCATG TCATATTCAT TCTTGCTTAT GTTGCTTCCC TGTATTAGCC AACCACTTAC 1020
ACAGAAAATG ATGCCCTATA AGGAAAGGGA AAGATAACAG CTCTTAGTTT CTTTCCCTTT 1080
CAGTTCCTCC TTACTCATCA GTAAGCTGAA GATAGTGCTA GGAGGAACAC GTGCAATCAA 1140
GAAGTGAAAT AAAAACAGTT GAGTTAGTTT TGTGCAGTGT TTCTACTGTT CTAGTAAGAA 1200
CAAAACATAT GTGTGTGTAT AAGCTACAAT ATACAAATTG TGTAATTTTG TTGATTCTGC 1260
ATGAGTTAAA TACTCTGATA TTTTCATTTA AAACCGGCAT TGCACAACGG AAAGATGAAC 1320
ATTAAAATTC ATGGTAATAG TTTTAAATTT AAATTTTTCT TTATTCAGAA AAACATTAAA 1380
TAGCAAATAA AAAATACCAC TGCAAATCCA GGAAGAGCTC 1420
|
