| Tag | Content |
|---|
EnhancerAtlas ID | HS050-37251 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:85402090-85403540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr2:85402685-85402702 | AGGTACACCCTGTTCTT | + | 6.49 | | Ar | MA0007.3 | chr2:85402685-85402702 | AGGTACACCCTGTTCTT | - | 7.04 | | NR3C1 | MA0113.3 | chr2:85402685-85402702 | AGGTACACCCTGTTCTT | - | 6.06 | | SOX10 | MA0442.2 | chr2:85403018-85403029 | GTCTTTGTTTT | - | 6.14 | | Twist2 | MA0633.1 | chr2:85403394-85403404 | ACCATATGTT | + | 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 |
| GH02I085174 | chr2 | 85401720 | 85403770 |
|
Enhancer Sequence | TTGTTTATGT GTGTGGTTTT GTGTCTTTGA TATCGTTGAT TTGCCTTATG GCCTCAACCA 60
AACCCTCACT GTAACATGGC ACAGGCAGCG CCATGTGACA TCCTTGTCCC TGGCCCGCCC 120
GGCGCAGCTC ACAGTGGGCT CTCTGTGAAT GCTGGCTGGC TGAGTGTCTG GGAGTTGTGA 180
GCCCTTTGCC ATGTAACTGG AGAGGGTGGA AGTGTGAATG GAGACACCTG CTCAGTTGTA 240
CAATGCTCTT TGGACAGGGG ATCAGGTTTA AATCAGTTTG AAGCCTGCTT TACCACCCCC 300
TGCCCCCACA ATTGTTATTT CCTGAAAGCA TATGGTTGGC TGAGCTAGCT GAAAAATTAC 360
CCGAATTTTG ATAAAAATTT GAACCATGGA TTTCCTTTCT GACCATGCCT AGCTGTGTAA 420
ATTCCACAGG ATAGTAACAG GTGCCTGGCC ACCATCCAGC AAGACCCCTG ATAACGTCCA 480
TGCAGTGGGG AGCCACGGGG GCAAGTGCTT CCCCTCCCTC CTGGTCATAG GCTTGAGCAT 540
GGGTAGCCAG GATGGGGGGT GGGTGCAACT TGAGATAAGC AAATCGACAA CAATGAGGTA 600
CACCCTGTTC TTTGTCCTCT TGTCAACTTG TGATTTCCCG ATGGATCAGG TAATCCCCAG 660
TAGCAGATAA CTCAGTTGAA TTTTTTCACT GTCGCTGTTA TCTGTATTCA TTGTCTGCCT 720
AAATAGTAGT GAACAGAGAA AAAAAGAACA TTAAAATAGG AAGCTGGGAA TGACAGGAAG 780
AGGGACTGTA GGCCTGGTAA ACAAAAGTTG GCTGTAACAT GAGCCAGGAT ATGGAAGCGT 840
GACCAATACT TTGGACTCTC TCAATGCTGG CCCTCTGCGG TTCATGGCTC TCCTCCCTTT 900
CTCGCTGTCA CCAGCCACGT TTAGGTCAGT CTTTGTTTTT GGCTGTTGTT CCTGAAGACG 960
CATTTATCAG GTGGATCTCT TAAAATCAGG GTTAGGGATT GGAAGTCTAG CTGGGACAAT 1020
TCCTGTGAAG ACAGACTTCC TTCTGATGAA ATATTTACTA GCTTTTGTAG GAAGCCATCT 1080
CCTCCTCTTT GCTGTGATAA GAGGTACTCC CCACCTTTCT GTCTCATGGC AAGGGTGGAA 1140
ACTGATGATA TTTGTAGGGC ATACTGGGGT GAGCCAACAG GCTGGAGGCA GCCAACCCTG 1200
GGCATGCAAA GAAGCACCGT TTGGAAGCTC TGGTGTAGCT CTCGTGCAGC AGCAGTCCAG 1260
GCCCTGGGAC ATCTGAGTTT GAGGCTTCAG TCCTCCGCTG ACTGACCATA TGTTTACACT 1320
GCAGCCTGTT GTGGTATGAA ATGAGATCTG GAAGCACCTG AGCTCCCCAG TGTCTGCAGG 1380
TAGATGATTA TTTAATACCC TCTTCCCATA CATCTTCATG GTCAGGAGAC TGGACCTTGG 1440
CAATTCTGTT 1450
|
