| Tag | Content |
|---|
EnhancerAtlas ID | HS050-29500 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr17:60831720-60833570 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr17:60832130-60832142 | AATTGTTTGTTT | + | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH17I062754 | chr17 | 60832101 | 60832250 | | GH17I062755 | chr17 | 60832475 | 60832944 |
| Enhancer Sequence | ACTGCGCCCG GCCAAATTCT AACCACTCTT ACATCTCAAA TACAAGTGTC TTTGGTCAAG 60
CAGTGTTCTT ATGGAGACAT TAGCCCTGGA GTAGTTGGCG GTGTTGGGAG GAGGGTTCAT 120
AAGCAGCGGA AGGCCTGGGG ATTAACCTTT GCCTAAAGCC TGGTCTACAT CCAGGGTTTC 180
CACCCACCTA TCTACCTGGT GAGACTGGCA AGGATTCCAT TTTACTGATG AGGAAACTGA 240
GTTCAGAGAA GTTGTCCGCT CACATTTATG GGGTTATAAA GTGATAGCAC CAGGATTTGG 300
AGCCAAGACT TCATTCTGGG CTCTGCGACA ACCCCGAGCC CCCCTGTCTT GAGAGCATGT 360
ATCATAATAG AGAATATGAT TCTCTATTAA AAAGTGGGAG TATCCACTTA AATTGTTTGT 420
TTTTTTCTAA CTTGGCAGAT AGCTTGGAAA GTTCCTGGAC ACCAGTTGGA CTTGCCGCGA 480
AAACCATTAA TCTGGCCTTT CAGAGAAAAT CTTCAGAAGA ATGTATTTGC AAGGTGAATT 540
ATGAGGATTT AGGATTTGCC CTCAAATTTC TCTTTCAGGC TGCTCTTCAA ATAAATATTT 600
CCCCATCCAA AAGAGACCAC AGTTATTTTA GATGTTTGTC TCTTAACATC TGAATGCACT 660
GCTTTTTCTT AGCTTTACAA GAACCTGTCC TCACAATAAT CCACTCTACA GCTGAAAAGT 720
CTTCTTACTC CTGCAAATCT GAACCCAGTA ATGACTAACA TTGCACCCAA TAAGAAGTGA 780
GGATAATTTC AGAACACTTG GCTTTGCTTT AAAGGGCAAG ATTTTGGAAG CAGGTTCACA 840
GGACTCCATC CAGATCTGTC TTCCTGGCAC ACAGCTCAGG GGACCATGCC CAAGCTCCAG 900
GTGACAGCAG AGGGCAGGAG AGGGGACGCT TGCTTCCCAC ATGTCTGGCC CTAGGGTAGG 960
GAGCTCGTTA GGACTCCAGG TGCCAGAATC CCACAGCACA GTGGCCTCTG GATGCCCCTT 1020
CGTGTCCTGG AAAGGAGAGG CGGCTCCTCT CCAACTCAGG GTGGGGCTGG GAGAGGTCTT 1080
GACAGCAGGC AGGCCTTGGA GGCCACCGCA GCTCCCCAAA TGTCCCTGTG CCTCTGCACT 1140
CGCTGGGCCT GCTAGCTGTT CTGGGTCTCA AGGGTATATA TACAATTCTG AACATGTAAC 1200
TAAGAACATG TAACTCCACT AGGCTCATAT CTCACCCTAC ACCAGCGTTC ATGATGTGGG 1260
ATTTCTGAGC TGACTGCACG TGAGACCCGG CCAGGTCTTG ACTCACTGCC TGAATTTTCC 1320
ACGTCTTTCT GGAGATAAAG CCTTTCTCTG GCTTGGTGAA TGCTGTCTGA TTCTTCATCT 1380
TTTTCCATTT GGCATTTTGC TTTGAAACTC AGAGTGTTGT AAAAGTAGTT GTACCTGCAT 1440
TTATGTTAGA GATTCTAAAA AATACAACTC TGAGCTGGGT GCTGTGGCTC ATGTCTGTAA 1500
TCCTAGCACT CTGGGAGGCC AAGGCGGGAG GATCACTTGA GCCCAGGAGT TCAAGACCAG 1560
CCTGGGCAAC AAAGCAAGAC CTCGTCTCCA TAAAAAGTAA AAAAAATGGC TAGGTGTGGT 1620
GGCTCATGCC TGTAACCCCA GTACTCTGGG AGGCCAAGGT GGGTGGATCA CCTGAGGTCG 1680
GGAGTTCAAG ACCAGCCTGA CCAACATGGA GAAACCCTGT CTCTACTAAA AATACAAAAT 1740
TAGCTGGGCA TGGTGGCGCA TGTCTGTAAT CCCAGCTACT CGGGAGGCTG AGGCAGGATA 1800
ATTGCTTGAG TCCGGGAGGC GGAGGTTGCC GTAAGCCGAG ATCGCGCCAT 1850
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