| Tag | Content |
|---|
EnhancerAtlas ID | HS136-00805 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:108583860-108585090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:108584948-108584969 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | NFIC | MA0161.2 | chr1:108584083-108584094 | TCTGCCAAGTA | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_56141 | chr1:108583407-108584252 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 108584232 | 108584689 | | chr1 | 108584121 | 108584359 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I108041 | chr1 | 108583966 | 108584915 |
|
Enhancer Sequence | CCACCTCCCT TTACATATTC TTTCTTTCCA TGCTGCCCCT TTAGGAAGGC AGGGGTGGTC 60
TGCCATTGGG CTTATCATCA GTCTCCCAAG AGCCCCGTGG TATACAATTA TGCCAAGCTT 120
CGGATTGCTT GCAGTAGAGT TGTCAGGTTA CTTTCAACTC CAGGCTTTTG GCACAGGGAA 180
GGCATTTGGC TGGACCAGGC AGGGGCTTTA ACTCGCAGCC TGCTCTGCCA AGTACAGTTG 240
ATGCTTCAGG CAAGAGGAAA GGAATTTGAA GTTTACTCTG GCTCCAGAAA TTCTGCTTAA 300
GGAACATCAG CAGTTAATAA AATTTAGTCA TTTTTTAAAC TAAGCTTACT GCTTTTTGTG 360
TGCTAATCTG TAATCTCCTC TTTTGGGCAA TATTTCAGCC TGCTTTGACA GCCCTGTTCA 420
GACTCCATTA ATCATAGAAT GTGATGACTT CCCTACTTTT CGATTTTTAA GATGCTTCAA 480
GGGAAATCTG TCTCCCCAGA CACTTGCGTA CTACATTGTA AGCCATTTTT ACTATGAAGA 540
AGATTGTAAG CTCAATTACG GGCTTTACTG CGCTGATAAC GAACACAGAT ATGAGACAAG 600
CAGACTTGAG CTCCTGCCTC GAGGATGGTG AGCAAAGAGC CTAAGCAAAA CTGAGAGGAA 660
ATGAAACACA AAGAGGAAAC AGAAAGGTGA GAAAATAGAG GGTGGGAGGG CAGGCAAGTG 720
ATTCATGGGG CCACCATAAA AGGGATATGT TAAGTGACCA AAGCAAAACC TCTAGAAAGG 780
GCTCAAATAC ATAAGATAGA GATCACATGG GGCTGTTCTG TCAAATATAG GGTGAGTGAT 840
GGGAAAGAAA ATAACTTGTT AAGGGAAGTT TCTAAACTGA GAAAATTTTG TGAGGTTTGA 900
ATATCTGTGA GACCAGTTTC GATCTAGAAC CAAGAAGTAG ATCCAAGACC TCCACAAAAT 960
GTATGTCTCT TCCCTGAGGA GAATGGGTTA AAATAGCCCA GACTAGGTAC AGAAATAAGG 1020
AGAAAATAGC AGTCCTGGAA GACCTAATTG GCCTATTAAC TTTTTTTTTA TTTTCTTTTT 1080
TCTTTCTTTC TTTCTTTCTT TTTTTTTTTT TTTTTGAGAC AGGGTCTCTC TTTGTCACGC 1140
AGGTTGGAGT GCAGTGGTAT GATCACTGAC TGCAGGCTTG ATCTCCTGGG CTCAAATGAT 1200
TCTCCCACCT CAGCCTCCTG AGTAGCCAGG 1230
|
