| Tag | Content |
|---|
EnhancerAtlas ID | HS044-12885 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr8:95809200-95810300 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr8:95809793-95809804 | TTTTATGGCTT | - | 6.62 |
| | | 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 |
| GH08I094796 | chr8 | 95809113 | 95810752 |
| Enhancer Sequence | ATCACTTGCT TTCAGCCTCA AGAACTTCCT TTAGTAATTT TTAAAAGATG AATCTGTTAG 60
CAATGAACTT CCTCCGTGTT TGTTTATCTG GGAATGTCTT TATTTTGCTT TTTTAAAAAG 120
ATCAGTTTTA GGCTTACAGA AAAATTGGAC AAAACATACA GAGAATTTCC ATACACTCGG 180
GCTCCCCTCC GCCCATACAC ACACAGTTTC CTCTAACTCA ACACCTTGTA TTTGAATGGC 240
ACATTGCTTA CAATTGAGGC AAATTGACAA ATTATTATTA ACTAAAGACT ATAGTTTACA 300
TAGGGTTCAC TCTTTGTGGT GTACTGTTCT GTGGGTTTTG ACAAATGTTT CTATGGGTCT 360
CACATGTCCA CTATCACAGC ATCTGGAGTA AGCAGTTTTA CTGCCCTAAA ATTCCTGTGT 420
GCTCTCCGTA TTCATCTCTC CCTCCCTTCC CGAGTCCCTG GCAACCACTG ACTTTTTACT 480
GTCTCTGTAG TTTTGCCTTT TCAGAATGTC AGCTGTTTGG AATCATGCAG TATGCAGCCT 540
TTTCAGATTG GCTTCTTTGA CTAGCAACAT GCGTTTCAGG CTCCCCCACG TCTTTTTATG 600
GCTTCATAGC TCATTTCTTG TTATTGCTGA AAAACATTCC ATTGTATGAG TATGTGGGCG 660
TTTATTTATT CAGGGACATC ATGGTTGCTT CCAAGTTTAG CCATTGTGAA TAAAGCTGCC 720
ATAAATATGT GCAGGGTTTT TGTGGACATA AGTTTTCCAC CCATTTGGGT AACTAACAAG 780
AAGTGCAATT GCTTGATGGT GTGGTACTAC TAACCTTTGG ATTAATAAGA AACTGCCGAG 840
CTCTCTTCCA AAATGGCTGT ACCGTCTTGC ATTCCCACCA GCAATGACTG AAAGTTCTGT 900
TGCTTCATAT CCCTGTCAGC ATTTAGTGGT GTCAGTTTTG GATTTTAGTC ATTCTAATGT 960
GTGTAGTAAC CTGGAAGTTC TGCTGGGCTC TGCCTCTGCC TCTCATTGTT ACTTTAAGTG 1020
ACAATTGCCT AATGACATAT GATGTTGAGC ATATTTTCGT ATGCTTATTT GCTATCTGTA 1080
TATCTTCCTT GGTGAGGTAG 1100
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