| Tag | Content |
|---|
EnhancerAtlas ID | HS050-03292 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:92066980-92068290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Twist2 | MA0633.1 | chr1:92068255-92068265 | ACCATATGTT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAAAAACAAT GCATGAGTGG ATGAATTTTC CCAGCAATAT TCCTTGGCTC CCCCATTGAC 60
CAAAAATGGT ACCATGAAAG ACAAACCTGT AACCCTGCCC CTGTCTCAGT CATTTGTGTC 120
ATTGTAAGGG TTTTGTTTTG CTCTGTTTGG AACAATTCTT TGGACACAGA CAATTCAACT 180
CGAGCAAACT GTACTCAAGA GGTGGCAGTG AGCGGTCACT GCAGCCTTGG AAAGGCCCTG 240
CCTGGCACAC ATCGCACTCA CTTAGGATGC CTCCACATCC CCAGTCCCAG AAGAGGTGAG 300
GAGAGAAGGC AGCTGCTGAC AGGAGGAACT GGGACGGTGT CACCGCTGGT GGTGATTGAT 360
GCCCCTGTCC TCGCTTGCTC ATTCCCTGCC GTTGCTGCTT CCTCAGCAGG GGAGGTGCCC 420
TTCCTAGCAG GTCCACCCTC CCAGCACGGC CTCTCCCAGG GCCTCTCACC AGTTCATCAG 480
CCCTCACCAC TCTCCCTCCA AACCCTGGAG TGCTGACAGG TGCCCAGGAG AGAAAGGCAT 540
GGGGACGGAT TCTGGGAGCT GACTCTCATG GTTGTTTACA CTGAGATGAG AGTGCGGGGG 600
TCCCAACCAA GCTGTGAACA AGCCCCTGCT AGGAAGATAA GCCCTGAGGG AGATACATAC 660
ACACACACAC AGATACACAC ACACACACAC ACAGATACAC ACACACACAG ATACACACAC 720
ACGCAGATAC ACACACACAT ACACACACAC ACACACACAT GCCTACAGGG AGTCTTCCTG 780
GATGGAGCTT TGGCCACAAG CTCTCCCTAG TTGTCTCCCG GTGAGATAGA AGGAGCCAAG 840
TATTTTTACA GGCAATAGGC AGGCCTGAAG CCTTAGTGAA AATCTGGCTG AGGGTGGCCA 900
GCACCTTCAT CTGAGCACTC TAGACTTTGC CATTCTCTAG AAAAAGAAAG ATAAATCCAA 960
GAAAAAAAGG AGGAGGCTGT TTGCCCAGTG AGGCTCTCTC TGACAACACA GCCCTACTCA 1020
ACTTTGCTCC GTGGTGGTCC AGATGGCCCA GGTGGCGGGG AAGCTCCCCT GGGGCCCAAC 1080
GAGGGTGACA TGGAAAAATT TTAAAACTCT GCAACACATA TATCAACTGG CTGCCAGGAC 1140
TGACTACATA ATTCGTTGGG CCCAGTGCAA AATGACAACA TAGAGTTTCT TACTAAAAAA 1200
GCAGGAAAAA AGGCCTTTAA AAATATTGAA ATATGAAACA TTTTTCTTTC ATGTACTTTT 1260
TCATGGTCTA TATTCACCAT ATGTTTTTTA TTTGCTATTT AATGTTGTTC 1310
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