| Tag | Content |
|---|
EnhancerAtlas ID | HS051-16246 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:171363490-171364820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:171363897-171363918 | TCTTTCTTTCTTTTTCTTTTT | + | 6.87 | | Myog | MA0500.1 | chr2:171364216-171364227 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr2:171364216-171364227 | GACAGCTGCAG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 171363796 | 171364070 | | chr2 | 171364162 | 171364651 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I170507 | chr2 | 171364221 | 171364350 |
|
Enhancer Sequence | TTTCATTTCT ATTTCTTAGA TCCCTGGTCA TTTCACACAA AAGCTAAATT CTTCAAACTC 60
ACTGTCTTTA TCAGAGGAAG CACAGGTGTG AGAGAAGACA AGATCCAAAC TCTTCTTGGC 120
CGTAGGGCAG GAGGCAGCTG CTTCTCTTTT CCTGGTGTTT TCCGTATCCA CATATCCACA 180
GAATAGCAAT AAAACATCTG GGGGAAATAA TTTACCTGGT GCACCTGAGC TTGAGATGCA 240
CTGTGAACTG CAAACTAGCC CTCCCCATCC GCCTACCCCC CCATCTTCTA AACCTTTGTT 300
TAACACAAGA CAGGATGCCC TTCAGTCCTA GGCGAGGGGT CCTGCTCACT TCACTCTCAT 360
GCTATCTTGG TTTCCCTAGC TCTCCCATAC TTGAGAAAGT GGGGCTTTCT TTCTTTCTTT 420
TTCTTTTTCT TTTTTTTGAG ATGGAGTCTC ACTCTGTCAC CCAGGCTGGG GTGCAATGGT 480
GCGTTCTTGG CTCACTGCAA TCTCCCCTTC CTGAGTTCAA GGGATTCTCC TGCCTCAGCC 540
TCCCAAGTAG CTAGGATTAC AGACATGCAC CACCACACCC AGCTCTTTTA TTAGTAGAGA 600
TGGGGTTTCA CCACATTGGT CAGGCTGGTC TCAAACTCCT GACCTCAAGT GATCCGCACG 660
CCTCAGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCTA CTGTGCCTGG CCTGGGGCTG 720
ATTTCTGACA GCTGCAGGCT TAACATATCT TGTAGGGGGA AATGTCTAGG GGGAAAGCAT 780
TGTGGTTTAC TTGAGGAAAA CATACCTTGT CTGTGACAAG GCTTAGAGCA AGTGGTGTAG 840
TACAGAGACA GGATGGCCTG TGGTTTCGAG GTTTCTGACA AGAAATGAGC TCTGCCAAAT 900
CTCTCTTTGG CACAAACGAT AGAATTTTTG TCATGGCATA GCTTGGAATG CACAGGAATC 960
TCCTTTGCTA TGGAATAAAA TTATTGCCCA TGCTAGGATT AAATAAGCCA GAGGGCAGAA 1020
TACTGTTTAC CTAATGCACA GAGAGGAAGC TGCAAAGTCA TTGTGGGCTG GAGGTCCACT 1080
TGTGCCCAAT ATCATACCGG CATGGCACAA GTATGCTTAA GATGAAACTT TTGTGCAACA 1140
GTAGGTACCC CTAGGACTCG ATATTATAAC TTCAGAGGAC GCCAGGGTTA GAGCCTACAA 1200
TCTGGAATCA GTTTTCTCCA TTATGAACCT TGTTTAGCAT TCCAGAGTCT AGCTGCAAAG 1260
AAGTGGTGCC TGAAAAGGTA TCTTTGCCAC CTCAACACAG AATGAAACAA CATTATTATG 1320
ATCGATTACA 1330
|
