| Tag | Content |
|---|
EnhancerAtlas ID | HS050-38215 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:128658640-128659660 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr2:128658804-128658819 | GAGGTCAGGAGTTCA | + | 6.22 |
| | | 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 |
| GH02I127901 | chr2 | 128659381 | 128659550 |
| Enhancer Sequence | CTGGAGGTAG GATCTTCAGG AGGTAATTAA GGTTAAATGA GGCCATCAGG GTGGAGCTCT 60
AATCTGACAG GATTGTAGCC TTATAAGAAG AGGAAGGAGT GGCCGGGTGC AGTGGCTCAT 120
GCCTGTAATA CCAGCACTTT GGGAGGTCAA GGTGGGTGGA TCACGAGGTC AGGAGTTCAA 180
GACCAGCCTG GCCAATATGG CAAAACCCTG TCTCTACTAA AAATACAAAA TTAGCCAGGC 240
ATGGTGGCTT GCATCTGTAA TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATCGCTTGA 300
ACCGGGGAGG CGGAGGTTAC AGTGAGCCGA GGTTGAACCA CTGCACTCCA GCCTAGCCTA 360
GGCAACAAAG TGAGATTCCA CCTAAAAAAA AAAAAAAAAA AAGAAGAGGA AGGGAGATAT 420
CCCCACCCCA GTCCTGCCCT GTGACGACAC AGGGAGAAGG CTGCTGCCAG CAAGCCAGGA 480
AGAGGGTCCT CAGCAGAGCC AAGTTGGCCA GTGCCCTGAT CTTGGATTGC TGGCCCCCAG 540
AACTGCAAGA AACGAATGCC TGTTGCTTGA CCATTCAGTC TGCAGGATTT TGTTAAAGCA 600
GCCCAGGATG GCCAAGACAG CTTTGGAAAT GAAAATGGCC ACTGTTCGCT ACGGAGAAGA 660
GACCCTCATT CTAGACTTGT GACTCTCCAA TTCTGCACTC CCATTTAATT TCCCCAGTGC 720
TCTATTTAGA ACATATCCTC AGGGCCTGCC GATGCTAGTC ACTCTCTGGA AGCCTTGCTT 780
CTAGAACTCC TGGGAAATTT CAGCTCTGGC ACAGACAGCT CTGGCCTTCA CGTCAGGAGG 840
CCTGGATTTG TGCCCGAGCT TTGCTGCTTT GCCTTCAAAT AAGACTCTTT CCAGCTCTGG 900
TCTCAGTCTC CTCATTTGTA GAATAAAGGA ATTGGATTAA ATTTAGGGTA TTTAACCAAA 960
CACCGCATGT TCTCACTCAT AGGTGGGAAT TGAACATGAG AACACTTGGA CACAGGGTGG 1020
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