| Tag | Content |
|---|
EnhancerAtlas ID | HS050-28428 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr17:33467820-33468990 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr17:33468348-33468363 | GAGGTCAAGAGATCG | + | 6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGGTCTCGA ACTCCTGACC TCTAGTGATC TGCCCACCTC AGCCTCCCAA AGTACTGGGA 60
TTACAGGCAT AAGCCACTGC ACCCGGCCTG AAATTCTTTA TCTGCATCTC ATAACAACCG 120
TGGGAAGTAG ATACTAATAT TCCCACTGAC AGTTTTCAAA AGCAGAGGCT CAGAACAACT 180
AAGTAATTAG TTCAATGTCC TATTGCCAAT GATTAATTCA GGTTCTTTAC GTCCAAGATA 240
GGATTAGCAT ATAGCATTAT GCAGTGTTTC CCAAACTACC ACACTACACT ATATTTGTGT 300
AAAAAGCTCC CAAAACGCCT GTTAAAAAAT GTAGACTTTC TGCTTCATCC CAGAGTTTGG 360
TTTAGTAAGG CTGGGATGGG GTCCAGGAAC TGCAATTTTA AGGACCTCCC CTGTCCCCAG 420
GGCAGCTCTT CAGTAAACAC ACTGGCTTAA AGGTTAAAAG CAAAGGCCGG GTGCGGTGGC 480
TCACGCCAGT AATCCCCAGC ACTTTGGAGG CCAAGGCGGG AGGATCACGA GGTCAAGAGA 540
TCGAGACCAT CCTGGCCAAC GTGGTGAAAC CCAGTCCCCA CTAAAAATAC AAAAATTAGC 600
TGGGTGTGGT GGCGCGCGCC TGTAGTCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATCG 660
CTTGAACCTG GGAGGCAGAG ATTGCAGTGA GCAGAGATCA CGCCACTACA CTCCAGCTTG 720
CCAGCCTGGC GACAAAGTGA GACTCCGTCT CAAAAAAAAA AAAAAAAAAG GTAAATAAAT 780
AAATAAATAA AAGCATGGGT ATTCGGATAG TTTTGGGTTC CAATTCCAAA TCTGCTACCT 840
ACTACATAGC ATCGTGCAAA ATACTGAGTC CCTCCGGGCC ACGCTGTAAA ATGGGGATAT 900
TAACGTGTCC CAGACTGGGG GACTGTGACA AAGAATCAAT GAAATACAGC ATCCGGTGCG 960
TTCAAAGCTA GGCCCCTCTC CGCAGGTGGA CCCCTTTGGT TGGCGTGTAA AGCGCTATGC 1020
CACTGATTCC ATCTCTGACA TAGGTGGGAG CTCACGCCAG GTGGGTCACC ACAGTCCGTT 1080
AGCGGGGGAC CATGAACCGC AGACCCTCGG TAATATGATT CCCCCACCGC ATCCGCCCGG 1140
GGGTGGAGAT GCGAGGCCGC CCTGGCCAGC 1170
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