| Tag | Content |
|---|
EnhancerAtlas ID | HS050-05790 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:213097700-213099120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr1:213097772-213097782 | GGCACGTGTC | - | 6.02 | | IRF1 | MA0050.2 | chr1:213099099-213099120 | AGAAAGAAAGAGAAAGAAAGG | - | 6.59 | | Npas2 | MA0626.1 | chr1:213097772-213097782 | GGCACGTGTC | + | 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 |
| GH01I212924 | chr1 | 213097868 | 213099407 |
|
Enhancer Sequence | GACCGAGACC ATCCTGGCCA ACATGGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAATTA 60
GCTGGGCGTG GTGGCACGTG TCTGTAGTCC CAGCTACTCG GGAGGCTGAG GCAGGAGAAT 120
CGCTTGAACC CAGGAGGCAG AGGTTGCAGT GAGTCAAGAT CGTGCAACTG CACTCCAGCT 180
TGGTGAGAGA GCGAGACTCC ATCTGAAAAA TAAAATAAAA TCCTGTGCAT TGATGTATTC 240
CGTTTCTTGG AGAAGTCTCC GATGATGCAC CTCCTTGGAT GCCTCCCTCT GCTCTACCTC 300
TTTGTCCCTT GCCACTTTGT TTCTGGCCTT CCTTCCTCCA CCTGGCCTCT AGCCCGTTCA 360
TTCTTCTTTG GGCTAGTCCT CCCCAGATCA TCACTGCCCC ACTGAGCTGC TCCCCAGCAA 420
GACCTGGAAA TAAGTGAATT TTTGACTCCT CATTTTTCAC TCCTTCATCC TTGTGACTTC 480
CCTCCAGCTC TGCAAAGGGA GGGCTGGCCC CAGAGGATCC GGCTCTGTCT CCCTCACAGC 540
TGGCAAACAG CTAACTTGAG TCATGGCCTT GGAACACAAA TAATCTGTTC TCATTTATTT 600
AAAAAATAAA ACAAACCATC AGCAGCCAAA ACAACACACT GATAAAGGCT TTGGTGAAAG 660
ATGATCCAGA GTAGATAAAC TGTTCCTTAA TCAGCAGTGT GGTAAATAAA ACCCCTCTTG 720
GGGAGCCTTG CTGAGGGTAT TTTGGGCAGC CTGGAGAGTT TTTAACCCTC ATTAGCCCCA 780
ACTAAAAATG GAGCCACTGG AATTTCTGCA CGCAGCTGTT AAGCAGTGAG TAGGACTTTG 840
AGTGTGTTAT TACAAACACT CTTACTGATT ATGCCTCCCA ATCCCTCAGG AGCAGAGGAG 900
GAGGCTGTTT TGTGCCTATC TTCCAGGGCT GAGATCACTG CTGCTCTCAC GGTTTCCTGA 960
CAATTTCTTC ACCTCCCAGC CATTCCCTTG GGCTGAGTAG AACATCCCCT GCTGCCTTTT 1020
AGAACTTTGC CAATCATGGC TGGGCATGGT GGCTCACGGC TGTACTCCCA GCACTTTGGG 1080
AGGCCGAGGC AGGCGGATCA CCTGAGGTCA GGGGTTCAAG ACCAGTCTGG CCAACATGGT 1140
GAAACCCCAT GTCTATTAAA AATGCAAAAA TCAGCTGGGC GTGGTGGGGG GCACCTGTAA 1200
TCTCAGCTAC TTGGAAGGCT GAGGCAGGAG AATCACCTGA ACCTGGGAGG CGGAGGCTGC 1260
AGAGAGCCGA GATCACACCA GTGCACTCCA GCCTGGGCAG CAGAGTGAGC CTCCATGAAA 1320
GAAAGAAAGA AAGGAAATGA AAGAAAGAAA GAAAGAAAGG AAATGAAAGA AAGAAAGAAA 1380
GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA GAAAGAAAGG 1420
|
