| Tag | Content |
|---|
EnhancerAtlas ID | HS051-15002 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:26963140-26964600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:26963620-26963630 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr2:26963620-26963630 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr2:26963620-26963630 | AATGGAAAAT | - | 6.02 | | NR2F1 | MA0017.2 | chr2:26963532-26963545 | CAAAGGTCAATGG | + | 6.2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 26963213 | 26963516 | | chr2 | 26963762 | 26964154 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I026740 | chr2 | 26963801 | 26963950 |
|
Enhancer Sequence | CACATGTATA TACATCTGTC AACTTACCAA ATTCTGCATT TTAAATATGT GTAGTTTATT 60
TTATGTCAGT TTTATCTCAA AGAAGCTGTT TAGGAAAAAA CAAACCATAG AGGCTTTGCA 120
CACGGCCCAG CAGATGAGCT AAGCACTCCC ACCTACACCC ATTTTGTTCT GATGGCCACG 180
GTAGGGGGTG TAAGTCCCCC ATGCCTCTTT ATGAGAGGGT CAGCGGGGAG GCCATCAATG 240
CTTCTGGTCA ACTTCTGCCC ACCCCAGACC AGGCCAGCTG TCGGCACAGG TGTCGCTAGT 300
GTCACTCGAA GCTGGACACA TATCAGTATA TGGATGTAAC AAGCAACCAT GAGGTCCCCA 360
TGGGGTGTTG CTGGCACAAG CCAGACATCA AGCAAAGGTC AATGGGGCAG GAGCTAATCT 420
AAAACACTGT GCCTCTGCCT AGGCAAACAG GGTCTCTCAG GCCCTAGCAG GCTGAGGGTA 480
AATGGAAAAT CCCCAGAGCC CATGAAACCC CATTTCTTTG GCTGTTTCTT CGCCTATTAA 540
AATTACTCTC CCATCTTTTT CGAGGAGTCC CAAAGGGTCT CATCCCATCT AAACCACTAT 600
GGGGTAACCT CTGCCTAGGC TGGCACGCAC ACCAGGGTGA GGGACAAGGC GCCATGTGGC 660
CCAATCGTTC TGCCACCTGC CGCTTGGGGC TGGAGCTGCT CAAGGAGACA GGCTCCTCCT 720
CGCCTACAGC TGTCAAGACA GGCGGACCAT CCTGCTGCTC AGGCTGCAGA GTCTGCCCCA 780
ATGAGCACAG TCCTCAAACC CCACCCACCT ACTGTGACAC TCCCTCCTGC AACTTCAGAG 840
CATGTTGTCT GGTGCTCCAA ACTTTCGTGG TGGGTTTAGT GAAAACGCTT TGGATTTGTA 900
CTCACAGCCC CCTCTCTGTG ACTTAGCCCT CTCTCCTGAG TGCATGAGGA CTGGGCTGTG 960
TGGCAGGAAC CATACAAACC TCAGTGCTAT GCTCTGCTAT GCTTTTATTT CCCTTGTGGT 1020
CTGCCTGCTT CCCTTCAGAT GAGGCTGGCC AAGAAGCACC ACAGACCCTG ATGCAAAATT 1080
GCCCCTAAAG CACTTCAGCC CGACCAGTCA GGTCTGCATT CCTGGATAAG CCCAATGCTG 1140
ACCCCATGGG GACCCCCACT CCCTTCTCCA GTACTAGGAG CTGGGCCCCA GGGAGGGACT 1200
TGGATAGGAC CCGCTCGTGT CTGCCACCAT GAGTGTGAGC ACAGGGCTGA TGGAGCTTTG 1260
CAGAGAGAAA TGAAGGTCAA GGTGTGTGGG CTGAGTGCCA AGTGAGACAG AGAGGGCTCC 1320
AAGGCTGGGG AGGTGTGGAC ATGGGGCCGG GGCTGGGCCT GACTGAGCCT GGAAGGAATG 1380
GTGGGATCTA GCACATGGCA ACAGCATTTC AGGTGTAGGA AATTGAGCAA AGGCCCCATA 1440
GGGGAATGTT CCCAGAGTGC 1460
|
