| Tag | Content |
|---|
EnhancerAtlas ID | HS136-01413 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:179186540-179188060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr1:179187275-179187290 | GAATGAGTCAGCAGA | + | 6.22 | | Nfe2l2 | MA0150.2 | chr1:179187273-179187288 | AAGAATGAGTCAGCA | + | 6.79 | | Nr2f6(var.2) | MA0728.1 | chr1:179186544-179186559 | GAGGTCAGGAGTTCA | + | 6.22 | | SPI1 | MA0080.4 | chr1:179187299-179187313 | TACTTCCCCTTTCC | - | 6.22 | | SPIC | MA0687.1 | chr1:179187299-179187313 | TACTTCCCCTTTCC | - | 6.49 |
|
| | 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 |
| GH01I179217 | chr1 | 179186681 | 179188308 |
|
Enhancer Sequence | ACCTGAGGTC AGGAGTTCAA GACTAGCCTG GCCAACATGG TGAAACCCCA TCTCTACTAA 60
AAACACAAAA ATTAGCCGAG TGTGATGGCA TGCACCTGTG GTCCCAGCTA CTCGGGAGGC 120
TGAGGCAGGA GAACCGTTTG AACCCAGTGG GTGGAGGTTG CAGTGAGCCT CGATCGTGCC 180
ATTGCACTCC AGCCTGGGCA ACAGAGCAAG ACTCCACCTC AAAAAAAAAA AAAAAGAAAA 240
GAAATATTAG TAACACTAAG CCTAAAGATT AAGACAGGAG TTCAACATTA CCATGAGATT 300
CCAAATGGTA TGGTGAGTTC CCACCTCTCC TTCATTAGAC CATCATATAT ATCTAAGACT 360
CAATCCATAG CCACATACTA TACAAATCTA ACCCTGGTCT ACCAGTCTGA AAACCTCATC 420
ACTGGTCAAG ACAGATGGGG TAAAAAATAC CTAAAAATCT TTGTATTATA TATATACATA 480
CATATGTATA ACTACATACA CACATATTCT AAAAGGTAAC TAGGCACCAG CATATACCAA 540
AACTATAGAA TCACAAACAG ACATCCCATC TTCTTTGGTC TCTAATATTT TTTAATTTGA 600
GCAACGAGGG TTTTATGAGT TTTAAAAGAA AAAACAGATA TTGAGTACTT AGAACATGCC 660
TGGCACACAG CCCTCAATAA ATGGCAATTA TTTCATTACC CAATTCTTCC AGGAACTGTA 720
GCCCAATCTG CTCAAGAATG AGTCAGCAGA ACTGTTTTCT ACTTCCCCTT TCCCTGATAA 780
CTCCAGATTT TTTTCAAAAA TGTGTCTCTC AAGAGACCTC TAATGTACGA ACTTTTAGAG 840
ATAAACCACC AAAAAAATGG TATAAGACTG TGGTGACTTG CATGTGGACA CTAATAGGCT 900
AGGAACAAAT GAATTTCTGA ACCAGTTTTG AAGAGAGTTA GTACATTACA TCCTGTTTTC 960
TGACAGTCAT TCAATCACCT CTGATCAAGT ACTCTTTTCT TTTCTTTTTT TGAGACAGTC 1020
TCGCTCTGTC ACCCAGGCTG GAGTGCAGTG GTACGATCTC GGCTCACTGC AGCCTCTGCC 1080
TCCCTGGTTC AAGCAATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGACT ACAGGCGTAC 1140
GCCACCACGC CCAGCTAATT TTTGTATCTT TAGTAGAGAT GGGGTTTCAC CATGTAGGCC 1200
AGGAGGATGG TCTTGATCTC CTGACCTTGT GATCCACCTG CCTTGGCTTC CCAAAGCACT 1260
AGGATTACAG GCGTGAGCCA CCACACCAGG CCAAGTACTC TTCTTAATCT CACATGAGCA 1320
GGAGATTCTC AAAGCATGGT CCCCAACCAG CAGCACCTGT AACACCTGAA AATTTGCCAG 1380
AAATGCAAAT TCTTGAGCTC CTCCTCAGCC CTAAATCAGA AACCCTGGAG GTGGGACCCA 1440
GCAATCTGCT TTAACAAGCT CTCCACGCTC AAGTTTCAGA ACTGTTCTAT ATGATTTGAA 1500
GTAGCTACAT ATTTACCTCG 1520
|
