Tag | Content |
---|
EnhancerAtlas ID | HS187-11476 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr18:47314770-47315950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr18:47314809-47314819 | ACCACGTGCT | + | 6.02 | Stat6 | MA0520.1 | chr18:47315507-47315522 | TATTTCCTCAGAACC | + | 6.37 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 47315462 | 47315583 | chr18 | 47315649 | 47315703 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH18I049788 | chr18 | 47314803 | 47315838 |
|
Enhancer Sequence | TTATTTTGTC ACGTAGTTAA AATACTCTTT GGACAACAAA CCACGTGCTT ATTGATTAGG 60 ACTATCCAGT TAATGCACTT CAATTTAAAA TGCCAGTTTC ATGTGGCTAC TGATTTACTA 120 CAGCTACTGA TTTACTACAG GATCTGATTC CAGATTCTCT TTGTATGTCT AAAGCATGAA 180 ATCATGAAAA TGAGATGGGT AGTCAGTAGT AAAGCATCAG TTATCCAGCC TGGTGAGGGG 240 ATGAAGTAGC CAACAGTGGT GACAGACACA TAAAAGGTGG ACAATGTTCA GACCACTGTA 300 CACACTTCCT TGTCTGCATA AACAACACAG CAAGCATGAC TCGTACTTTC ACTTTAACTC 360 AGAATCCACC GTAACAATAT GCTAGGCCAT AACTCGATTT TTAAAGGACT CTTCCCAGAC 420 CACTGTTATT TACTGGGACT TCAGGAAGGT TTAGTATTCT TGTTAGGAAA AGGAGACCTT 480 ATTTCTAGTC CTGGTTCCTG TCACTAATAG CTGTGCGACT TTGTGCATCT CTCTGGGCAA 540 CAAGCTACTC ATCAATAGCA CTCTGAATGG GTTTTCCACC TTTTTCTCTT TAAGCATCAG 600 AATTCTTTTT GCATATGATG CCAAGTAATA GATAATGCCA GACTGCTCCA GCTGAAGAGG 660 CTCAAAGTTC CACCCACCAA CCTCTACCAT TGCCACCCCT GAGGAGTTCC AGGGAGTGCT 720 GTCTTTCTAT AGCTGTGTAT TTCCTCAGAA CCAGTACTAT TCTTTTCAAG TCATGGCTTT 780 CCCCGTTTTT TTTTGGTCTG CAGCTATTCT GCAGGGCTAA GGATTGCTAG TCATTAGGTA 840 ATCATGGAAC TGAGAACCAC TATTCTTGTA AGTTAGATTA ACAAACCAGT TCCCACTAGA 900 TACTTAATAA CTTATTCTCC CCACTTATTC ATCTGGGATG CTTCAACGAG TTACTTTGTT 960 TAATCCCATC ACTATATACA AGTGACAGCC AAACTTCTAG ATGAAGGGGG CAGCTGATAC 1020 TGTGGGACAT CTGGAATGTA CAGCTCTGTT CAAGCCCCGA GGAAAAATGA CAATCCTACC 1080 ACAGGAGCAT TCTTTGTACT TTAGGGCAAA TATTCAGGCC CAGGAACAGA AGGAAGGAAA 1140 ACAACGCTTT CTTGGTTCAC TGGCTATGCT AATCTACCAG 1180
|