| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06378 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:121497590-121498740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:121497609-121497630 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | | IRF1 | MA0050.2 | chr12:121498035-121498056 | GAATGGAAACTGAAACTGAAC | - | 7.6 | | IRF9 | MA0653.1 | chr12:121498037-121498052 | ATGGAAACTGAAACT | + | 6.64 | | Zfx | MA0146.2 | chr12:121498683-121498697 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 121497704 | 121498735 | | chr12 | 121498035 | 121498283 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I121059 | chr12 | 121497290 | 121499130 |
|
Enhancer Sequence | GAGAGAGAGT TAGCTGCCCT TTTTCTTTCT TTTTTTTTTT TTTTTTGATA CAGAGTCTTG 60
CTCTGTCACC CATGGCGTGA TCTCAGCTCA CCGCAACCTC TGCCTCCCGG GTTCAAGGGA 120
TTCTCCCACC TCAGCCTCCT GTGTAGCTGG GATTACAGGC ACCTGACACC ACGCCCGGCT 180
AATTTTTGGT ATTTTTGGTA TTTTTAGTAG AAACGGGGTT TCACCATGTT GGCCAGGCTG 240
GTCTCAAACT CCTGACCTCA GGTGATCTGC CCGCCTTGGG CTCCCAAAGT GCTGGGATTA 300
CAGGCGTGAG CCACCGACGG AAGAATCACT AAGCTTACTT TCCTCTTTTT AGGGTGCAGA 360
GAGGGCTAGG GGGCCCTCCA GGCATCAGCT GAGCCTCCCT CTGCTGGGCT GCCTTAGTTC 420
AGCAGCCATC TCTCCTGCCG GCTGAGAATG GAAACTGAAA CTGAACTTTG TTTTGTTTGT 480
TTGGGTTTTT TTGTTTTGTT TTGTTTTGTT TTAATTGGAA ACAGAAAATT TGCTGAGCTT 540
TGAAAGAGGA ATTTTCTCTT TCCATTTGAG GTTGCCAGGA AAAAAGGCTG GAGATGGAGC 600
CAAGTGCCCC TTGGGCTTCC TTGAGAGGAA GGTTCTCAGG CTGGGAGTTT CCCAGGGTGT 660
CCTGGAGCTG GGCTGCCCCC ACCTCTCCAT CCCCTATTTC CTGCTGCAGG AGCAGACCTT 720
GTCTCCCTAC GGGAACTCAG TAGTGTCTGC CCCGGAATCA GAAGGTGCTG GCTCCTTGGG 780
GTGAGGGGAT GGGGGCTTGG GCTGAGCCCC GGGAGTCCTG GGGCCTGGGA TTGACTCTTT 840
ATTTTCTAAA AGCAAAGACA TACTCACCCC TTTACTACTT GTTTTGTTGC GTATATTTAG 900
GTCTCCCCTA TCCCCTCACC AATAATCCAC AGGAAGGAGG TAATCTTTTA AAAAATTGTC 960
TTTAGGGGGC GCTGTTCTCT CAAGAACTTC ATTTTGAAGA GCAAACTGAC AGTTTGTGGT 1020
AGACACATTG GCTTTTAAAG ATCTCAACTA GCGACCAGGC GCGGTGGCTC TCGCCTGTAA 1080
TCCAGCACTT TGGGAGGCCG AGGCGGGAGG ATCGCTTGAG GCCAGGAGTT TGAGACCAGC 1140
CTGGCTAACA 1150
|
