| Tag | Content |
|---|
EnhancerAtlas ID | HS136-10015 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr2:8369240-8370460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:8369998-8370019 | TCTTTCTTTCTTTTTCTTTCT | + | 6.14 | | IRF1 | MA0050.2 | chr2:8369988-8370009 | CTTTTCTTTCTCTTTCTTTCT | + | 6.95 | | NFE2L1 | MA0089.2 | chr2:8369899-8369914 | GCATGACTCAGCAAA | + | 7.91 | | NKX2-3 | MA0672.1 | chr2:8370433-8370443 | ACCACTTGAA | + | 6.02 | | Nfe2l2 | MA0150.2 | chr2:8369897-8369912 | CAGCATGACTCAGCA | + | 9.03 | | SOX10 | MA0442.2 | chr2:8369471-8369482 | AAAACAAAGAA | + | 6.62 |
|
| | 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 |
| GH02I008229 | chr2 | 8369501 | 8370496 |
|
Enhancer Sequence | GATGATGTGA TAACGTAAAG GTAAAATGTC TCTTCCAACT TGTAGTACTT CTTTAGAGCT 60
AACTTTTATT TCACTTAGAA ATGTGTGGAA GAGTTAATCC CTATAAATAG TAATAATTAT 120
TACTGAAGTA GAAACTTAAA TCCTTTGAAA TTTAGATTCT AAACTAACAT GCATTCTTTA 180
AATCATTTTA CACATGGTAT CCCTTGATAT TGGTGGTGAG AAAAAAGAAT GAAAACAAAG 240
AAATAGAAAA GAGGCAGTTC TTATATAATC TCACAGAAAA ATAGATTTCC TTGAAAACAG 300
TTTTTGGAGA GAAGCCTTGG GTCTGAAATA ATTCAATAAA ATAAACATCC TCTGAGCTAT 360
TCCTAATTTA TCTTTACTTG ATGGTGGTTG CAGATTGGAT TCTCCAGGAA GCAGATGCCC 420
AGATGGAGGT TGAGAGTCGA TTCGCTTTGT TAGAGACCGA CACCTATTAA GCAAGAAAAG 480
GGAGGACGCA GGATTGGGCA GGGTAGCTGG CAGAGAGCAA CGACAAATGA TGAAACAAAG 540
TCTCTGCCAG GGAGATCCAA GGCTAAGGTT GTCTTTGAGA AGTCCCATGT GGGGCAGAGT 600
CGGTTCTTTC TTGTTACCAC AACTTTGCAG GGGCAACCGG TAGGGCCGCC CTGAGAACAG 660
CATGACTCAG CAAAGCTGAG GCAAACCTCC AAGCAGCTGC AGCTGGAGAC TATGAGTTAG 720
CCACACTCTA CGCCTCAGGA AGCAGGTCCT TTTCTTTCTC TTTCTTTCTT TTTCTTTCTT 780
TCTTTCTTTT TTTTTAATTT GAGATCTTGC TCTGTCACCA GGCTAGAGTA TAATGGCGCA 840
ATCATAGCTC ACTGCAGCCT CAACTTCCAG GGCTCAAGTA ATCCTCCCAC CTCAGCCTCC 900
TAAGTAGCTG GGACTACAAG TGTAAGCCAC CATGCCCAGC TAATTTTAAA ATTTAGCTAT 960
CTCACTGTGT TGCCCATTCT GGTCCTAAAC TCCTGGGCTG AAGCAATCCT CCCATCTAGG 1020
TCTTCCAAAG TACTGAGATT ATAGGTGTGA GCCACCGTGC CTAGCCAGCA AGTCCATTTT 1080
TTAAAGGGAA TCTGAACAGC ACATCTCTGC ATCTGCCAGA CAGTAAATAA GACCAAAAAG 1140
GCAACAACAA AAGGGGTCTT ATGTTCTTCC TCATGAACAA CAGAACCTCA GTAACCACTT 1200
GAAAAGTTCT TTAACAAGTA 1220
|
