| Tag | Content |
|---|
EnhancerAtlas ID | HS136-10064 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr2:11327060-11328580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr2:11327471-11327485 | GTGAGTCATCCCTT | - | 6.29 | | Mecom | MA0029.1 | chr2:11328022-11328036 | AAGATAAGATAATA | + | 7.95 | | Nr2f6(var.2) | MA0728.1 | chr2:11328454-11328469 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I011187 | chr2 | 11327326 | 11327527 | | GH02I011188 | chr2 | 11328127 | 11328326 |
|
Enhancer Sequence | ACAGCATTTT ACATAGTACT GTAATTGCCT GTTGCTTGAC TGTCTCCACC ATTAACAGGG 60
ATATAGTTCA GGCCTGCGAA ACTTATTGTC AAAGATGCTT TGGAAAGAGT GCATTTAATT 120
TGGAGTTCTA CCAGCAGTCC ACAAAAGTAC CCATTTCGTT TCTTAACCCG TGCCAGTTTG 180
GCAGGTGAAA AATGGTTTTA TGTTATAGTT TTAATTTAAT GCTAATTTCT TAATACAGTA 240
GTCCCCCCAT ATCCTTGTCT TCACTTTCCA TGGTTTCAAG TTACCAGTGG TGAACCACAG 300
TCTGAAAACA TTAAATAGAA AAGCTCAAAA CAACTTAGAA GTTTTAAACT GCCCAACGTT 360
GTAAACAGCG TGATGACATC TTGTGCCATC CCACTCTGTC CTGCCTGGGA TGTGAGTCAT 420
CCCTTTGTCC AGCATATCCA TGCTTGTTAG TCACTTACTA ATGGTCTTCA TTATCAGATT 480
TTAAAAAATT GTATGTGTAC GGTCCAGTAC TATTCGTGAT TCCAGGCATC CACTGGGGGT 540
CTTGGACTAC ATATCCCTTG AGATAAAGGG GGACTACTGT AATCAGGCTG ATCACTTTTT 600
TTTACATTTA ACAGCTATTT CCATAATAAT GCCTGCATGC GCCTCATTAA TTTTGTATGG 660
GGATGAGGCA ATCTTTTTTC TCAATGATTT ATAAGAACTT TTCGTATGTG AAGATACTAA 720
CTCATCTTTC TCATATATTT TGGAAATACA TGGTGTTTTT TAAATTTACA AGGCTTTACT 780
TTTGGGGTAG TTGATCTTTG GCTTTGTTTT CTTTGCTTTT ATTATTTGGA AGTTCTTCCC 840
CAATTCAAGA TCAGGTATAT ATTCACCTAT GGATTTATTT TTGACACTTC AAATTGTATA 900
TAACTTCATT ATTTTCCCAA GTAGACTGTT AATTCTTTAA CATTTAGAAA TGAGGAAGAG 960
CAAAGATAAG ATAATAATGA CACAATAGCT ACTTCCTCCT TTAAGTTTTA ACTGTGCTGC 1020
CATGTTTTAC ACTTCTTAAA ACTCGGTAAG TGAGCATTTG TTACATTTTT GCTTTATACT 1080
TTTCTGCATG CATTAAATAC TGCGTTAAAA AAAATCTTTA AAAGAAAAAT AATTAAAGAG 1140
AAATACCCTC TAGCCAAACT GGTATATAAT TTTTTTTTTT TTTTTTTTTT TTGTGTGACG 1200
GAGTCTCGCT CTGTTGCCTA GGTTGGAGTG CAGTGGTGCG ATCTCGGCTT ACTGCAACCT 1260
CCACCTCCTG GGTTCAAGCA ATTCTCTGCC TCAGCCTCCC CAGTAGCTGG GATTACAGGC 1320
GCCTGACACC ACGCCTGGCT AATTTTTGTA TTTTTAGTAG AGATGGGGTT TCACCATCTT 1380
GGCCAGGCTT GTCTTGAACT CCTGACCTCA GGTGATCCAC CTGCCTTGGC CTCCCAAAGT 1440
GCTGGGATTA CAGGTGTGAG CCACCGCGCC CAGCCCAGAC TGGTATATTT TTATCTTGCA 1500
TTGAAACAAA TTAGGACTCC 1520
|
