| Tag | Content |
|---|
EnhancerAtlas ID | HS187-07114 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr13:114240790-114242300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr13:114242239-114242256 | CAGCTCACTGTGACCTT | - | 6.8 | | ZNF143 | MA0088.2 | chr13:114240860-114240876 | TTCCCACCGTGCATCG | + | 6.34 |
|
| | 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 |
| GH13I113586 | chr13 | 114240941 | 114241090 |
|
Enhancer Sequence | TATTGGTGTG CGGTTCTTTA CCGTGCTTGG TTATGTCAGT CACTGAAACA CCAGCTGGAT 60
TCTTTAGTGT TTCCCACCGT GCATCGTTTT GTAACTGAGT GAAAGGTGCT GTTGATGTGT 120
TTACCTACTT ACCGCACAGA GTTGGAAAGA GTCCGCACAT GCTGCCTCTG CCTGAGATAC 180
ATCTGTAGCG AAAATGCGTC CAGAGTGTGG AGCCCTCTCC GTTGGCGCAG AGGTTTCAGT 240
GGTCCCTGCG AGGCCTTTTG GGGTGTCTGC CCTCCCTGAC CTGCGACCAG GCATGTCACA 300
CGGCATCCCT GCCTTCAAGC ACTGGGGTCC CCTTTAGAGA GGGTGTGTGA GCACCCAGGT 360
GGACCCAGTG TGAGTTTTTG AAGTCATATC TGGCTGTGCT GCGAGACTAC TTTTATCCTC 420
TCCACTGTGC TTGTCCGTAC CATGCCCTGA CCTCGTGCGG GCATGCACTC AGAATGCCAG 480
ATGTGGGCAT GTGCTCAGCG CGCAAGCCAT GTTCATTACA TCTCCTCATG GTGAGGAGCT 540
GGACCCAGGG CCTCGGTTAG AGCACGCTTC TGGTGTTGTG TGGTTTCCTG TGTGGTTTCC 600
TCAGATGGTT CTCAAACACG CTTTGATACA TAATGGATGG TGTTTTCGGG GCCCTCTTTC 660
ATTCCCCCGT GATTTCACTG GCACTGTCTG TGAGCAGCAT GTAGTGTGAG GCTGGGGGTG 720
GGGGGCGTGT GGAAAGGTGG TCCGGCTCTG CAGGACCCTG AATGCTCCAT CCAGTGTGGG 780
CACCTGAGAC GCAGCATTTG TCAGGAACTG CATAGGCACA GGGGCTGGGG GCTCACCTTG 840
CACTCAGGGG TTGTGATCTG AGTTGGGGGT TGGCGCTGGG AGGAGAGTAG GATTCTGCAG 900
CTGGTGAGGC CTTCCCTGCT CAAAGCCTGG GAGTGGTCAG GAGTGCTGGG TCTGGATGGA 960
AAGTGAGGTT GTGAACAAGT CAAGGAATTT GATGTTTTCG CTAGCTCTTT TTTTTTTTTT 1020
TTTTTTTGAG ACAGAGTCTC ACTCTGTCTC CCAAGCTGGA GTGCAGTGAC GCGATCTTGG 1080
CTCACTGCAA CCTCTGTCTC CTGGGTTTAA GCAATCCTCT CGCCTCAGCC TCCCGAGAAG 1140
CTAGGATTAC AGGCATGTGC CACCATGCCT GGCAAATTTT TTTGTATTTT TAGTAGAGAT 1200
GGGGTTTCAC CATGTTGCCC AGGCTGGGCT CGAGCTCCTG ACCTCAACAA TCCACCCGCC 1260
TTACAGGCGT GAGCCACCGC GCCCGGCCTA GCTAACTCTT TTAAGTAGAG GTGTGACATT 1320
TGAGTTTTGA AAAGATGATG TTGGCAGCTT TTGCAGAAGG GAACATCGAT AACCAGTTAG 1380
GTGTTTTGTT TTTGTTTTTT GAGACGGAGT TTTGCTTGTT GCCCAGGCTA GAGTGCAATG 1440
GCGCGACCTC AGCTCACTGT GACCTTGGCC TCCTGGGTTC AAGCAGTTCT TCTCCTCAGC 1500
CTCCCAAATA 1510
|
