| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06147 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:102064750-102065890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr12:102064984-102064995 | ATTTTAATTAA | + | 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 |
| GH12I101671 | chr12 | 102064781 | 102066178 |
|
Enhancer Sequence | GGTCTTATAC AAATACACAC ACACACCCTG CACCTCCCAA CCCTTACTCT CCAACTCCCT 60
ATTCATATGA CACCTCCAGA CAGTGCTGTT CAATAGAACT TTCTTCAATG TTAGAAATGT 120
TCTATATCAA TGCTGTCCAA TATGGTAGCC ACTAGCCACA TGTGGCTGTT GAGCACTTGA 180
AACGTGTAAC TAGGAACTAG TGTGACTGGA GAAATAAATT TTTAATTTTC TTCAATTTTA 240
ATTAATTTTA ATTTAAATAG CCACGTGTAC CTTGTGGCTA TCGTATCAGC CAGCCTGGCC 300
TTAGAATGTA GGTCTCTACA CACATTTGAC ACTCATATAC ACACACACAC ACACACACAC 360
ACACACTCAC ACACACACAC TCACACATGC ACACATGCAC ACACAGAGAG AACTCTGTTC 420
AAACCCAGGC TCCCATGAAA CCAAACTAAA GGGATGGCCA ATTCAGGCCA TCCTCATTGC 480
ACTCCGGGTG CAAACCTAAG GAGAGACATT GTGTACTACA TACCCCCGGC ATGAAATCAG 540
AATGAAAGCC AAGGAGGAAG TGAAGCAGAA CACAGCCCAG GAGGAAGTGG GTGGCTTGGC 600
AAGGTTCTTC TCACTTTCCT TCTCTTGCAG CATCAAATAA AACCAGAAGT GGCAACAAGG 660
CAGGTATTGG GGACCCAGCC CCAACCCTGC ACTGGGGCTG CTGAGTCAGC CCTCAAGCCT 720
CCACATCGTT CCTGCCACCA CAACTAATCC CAGTTCCCAG ATCTGGGGGT CTGCGTGTTC 780
AGCTTCTGTC ACTGAGTCTG AGAGAGAAAA AATCATGAGA ACAGGGACCG CATAGATCTG 840
GCATCCCAGA GACTGTTCAG CCCCCAGGAA GGGAGATGAG ACCAAAGTGT GATGTTTGTA 900
TATTTGTGTA ATCTCTAGAG TTCGCAAACA TTTTCTCATT TGATCCTCAG AAACACCCTG 960
TGAGGCAGGA AGGCCAGATT TCCTTACCTT GCTTGAGAAG GGAAGAAACT GAAAGGGAAG 1020
TTAAGTGACT TGCCCAATGT CACACAGAAA GTCAATGGTA GGGCCAAGAA CAGAGTCCAT 1080
GGCCCGGTCA CTTAATTCAG TGGTTTTTTC CACTCTGTAT ATTATTAGAG AACCCACATT 1140
|
