| Tag | Content |
|---|
EnhancerAtlas ID | HS134-04036 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:182708130-182709500 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr1:182708834-182708849 | CTTGGCCTTGACCTC | - | 6.3 | | RREB1 | MA0073.1 | chr1:182709098-182709118 | CCAACACCCAACCCCCAACC | + | 6.01 | | TBX20 | MA0689.1 | chr1:182708854-182708865 | CTTCACACCTC | - | 6.02 | | TEAD1 | MA0090.2 | chr1:182709078-182709088 | CACATTCCAT | + | 6.02 |
|
| | 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 |
| GH01I182738 | chr1 | 182707891 | 182709380 |
|
Enhancer Sequence | GTATCTCTGA ATTTGATAAG CACTTAACTT CTGATCTCTC CTCACCCCTG AAATAAAGAA 60
TCTTATTGGA TCCTCTCCCA GGTATCTTCT AGCTGACATT TATGGCTTCT TTCCATTTAA 120
AAGTGGAATA TTCCCCCACA AGTGTGCTGG GAAAGTCTCA GCTTTCAGAT GAACAATGAA 180
ATATGCTGGA TACAGTCAGC TGCTACTTGG CTTCACCTTC TGCTCTTTCT CTAGTGTCAG 240
TACTTACTCC TCATCTAGGA AGAGAATCAG TGCTTAACGT GAGAGAAAAA GAACCCAAAA 300
GATGGCTTTC TGAGGGGCTT CGCACAGCCT GATAAGACAA TGTATTTTCT CCCCAACGCT 360
GTCATCTGGG GAAACACTGT CATCCCCAAC AGTGTCACTG GGGCCCCGAC CTTGAGTACT 420
GACGTGGGGG AACTGATGTT CTTTCAATGG GGTTTTTAAA GGCACACCAG CAGTCACAGG 480
CATACACACA GTTTCTGGCA TTTATGAAGA ATTGGGGTTT CTTTTAAGAG GAAAAAAAAG 540
AATAAACCAA ATTGTTCATT CCTTTTCTAA AGTATTGTAT ATTGGCTTTG TATTTGAGGA 600
CTGCCTTGTT ATCTTCATGT TTTCAGGCCT CCCCCTGTCC CATAGCCTAG GGGGAATCGC 660
CATGGCCCTG ATTTGTGTAT GTAGACAGTG CTGTTTCCAT TCCTCTTGGC CTTGACCTCT 720
GCCTCTTCAC ACCTCCTCCC ACTCACCCAG CCAGCGGGCA GCCCACCCAG AAGCCCTTGC 780
GCCAGCAGTT ACCTGGCAAC AGCGACAATC ACGCTAACAG GCAGCAACAC AGCAGCAGAG 840
ACCAGAGAGC TCTGAGTCTT CCAGAATCTA AGCAGGGAAG GGAAGGGGGG CAAACGGCTG 900
TTTTTATCAA TGGCTTTTCG TCCCTACCCA TACTGTTTTC CTGTCTCACA CATTCCATGC 960
TCCAGCTCCC AACACCCAAC CCCCAACCCC CAATTTCTAT CATCGCCTGG GTGAAACTAG 1020
CCTCCAATCC AGAGTTTAAT AACAGCCACA GAGATTCATA TGGAATTGTG TACTTGGGGA 1080
GACCCAATAA TCATCCCCCT TAATTCCAAT GCAGAATGCT CAGGAGTTAA TCAATCCTAG 1140
TTTCCATCTG TGCACATGTT GTGTTGCAGT CCAAGGATGT ACTTGACCAC CCAACTGGCC 1200
TGCTGTAATA GAGACCTAAG TGCTGTGTAC TCAGAAACAT TGACAAGCTA TTATCTTACT 1260
TCTTGCCTCC CTGGCCACAA TTCTACAGTA AGTGCTACCA GAGAGTGGGG CATAAGCATA 1320
CCAGTTAGTA ATAGCTAATA TTTACTGATA CTTATTCTGT TCTAGGCTCT 1370
|
