| Tag | Content |
|---|
EnhancerAtlas ID | HS136-20711 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chrX:1326790-1327690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chrX:1327568-1327580 | GAACAAACATTC | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 1326825 | 1327063 | | chrX | 1327097 | 1327494 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH0XI001207 | chrX | 1326825 | 1327063 | | GH0XI001208 | chrX | 1327094 | 1327967 |
|
Enhancer Sequence | CCTCGGTCTC CCAACGGTGA GTCTTATTTT CCAAATAACT TCGTTTTAAA ATTTCCCTGT 60
TCTGTACGCT TTGCCGTTTA TCTCTTTTGT TATCAAACTG AAGAATCATC CACCCATGAT 120
TAAATTTATT GGAAAAACCC TTCCTGCAAT GTTCGTACGC ATACTTCTGG GTGTCTAACT 180
AAGCCAAAGT AAAAATAAAA ATAAAGTCAC ATCAGGGAGA CACAGGGTTG GGGGTAGCCC 240
CGGGTAAGGC TGTGAAATGT TTCAGAGACT GAGTCTTTCC CTCCCCGGCT GCCTAGCAGA 300
TAAGACTTAA AGTTCACCCA GAGCTCTGGG TGAACAAAAC TCTCTGTTAA TCTCCCGTGA 360
AGAATCTAGG TGATTTTCAG TCCGGATGCC GTGGCTCACG CCTGTCATCC CAGCACTTTG 420
GGAGGCTGAG GCAGGTGGAT CACATGAGGT CAGGAGTTTG AAACCGGCCT GACCAATATG 480
GTGAATCACC ATCTCTACTA AAAATACAAA AATTAGCTAG GCATGGTGGC AGGTGCCTGT 540
AATCCCAGCT ACTCGGGAGG CTGAGGCAGG GGAATGGCTT GAACCCGGGA GGCAGAGGTT 600
GCAGTGAGCC GAGATTGCGC CACTGCACTC CAGCGTGGCA ACGGAGTGAG ACTCCGACTC 660
AAAATAAAAA CAAACAAAAA AAAGAATGTA GTTGATTTTG ACAGTGAGTC AGCCATCCCT 720
TGGCAAGAAG GTTTGGGGCA ATGAGATTGT GGTTGTGGTG AGGGCTGAGG GTTTCACAGA 780
ACAAACATTC CGGCTTGCAC AGTCTGATGC TTTACACTTT TGTTCTCAAG CATTCCCAAT 840
CGCTGACGGC TCAGAAGAGC GATTTTGAGC CCCCTGGGCG TGGGGTTCGC TTTCTGGGGG 900
|
