| Tag | Content |
|---|
EnhancerAtlas ID | HS044-00128 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr1:17058550-17060130 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Tcf12 | MA0521.1 | chr1:17059893-17059904 | CAGCAGCTGTT | - | 6.32 |
| | | 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 |
| GH01I016732 | chr1 | 17058895 | 17059496 |
| Enhancer Sequence | CCAGTCAGTG AAAAGTCTGA CTGAAAGCTG TCAACTGAAA AATCACACAA TTTATAAATT 60
TAGAAGGGAG ATTTTATTTT TTATAAATGG TTACAGCCTG CAAGGTGGCC ATTCTGACAG 120
ACAGGGAGGC ATACCCTCTT GCTGCTGAAA CCTGAAAAGT ACGTTTCCAG GGAGGGGAGG 180
GGGGAACAGG GATTTATGTT GATGTGGTGG GCCACATATA CATATTCAAC AGGGAATAGG 240
AGGAGCTCTG AATATTCATG AAGGGATCCT GCTGCATGCA TGCTGAGTAA ACATGCCTGT 300
TACATGCAAC CCATGTTCAT TTTGGGGTGG AGACAACATT TAAATACATT ATAATTAGGC 360
CCTATGCTTC AAAAGGGGAA GCAGGGACAC AAAGGCAGTC AAGTGCACAG CCTCTGTAAA 420
CCGTCCAGAA CCCGTCCACA GCCAGTGCTC TCTTATCAAG GGGAAGTTAC TGAAATCAGT 480
CTCTTGTCCA ATCAAAGCTG TAGTTATGGC TTGTGTAGGG AGGGCTCAGT CAGTTTATGG 540
TAATGGGTGA GCTGCAAGTG CTTCAGCATT GCTTATCTCA AGGCCAGTGC TTGTTTAGCT 600
AGAGAAAAAA AGGAAGAAGA AAAAAACCTG TGGCAATTGG AACATAGTTT ATTCTTTAAG 660
TTGAGGGGCG CATGACTCCA CCTTGCCTGG CGTGGCCTTA GGTCTCGTTT ATCATACCAT 720
ATCTTACTAC TGCAAGGAGT CTGTTCTGTC AGTCTTAGGA TCTCTATTTT AACAATAATG 780
CTGGTCAGTT GTGTCTAAAC CACAAAGGGA GAGAGTATAA GGAGAGGTGT CTGAGATTCC 840
AACTACTGGG CAGGAACTCA GTAGTTAAGA CTTCTCTGGG GTCTCCTTGG CCAAGAAACA 900
GTCTGTCCAG TTGGTTGAGT GGCTTTGGAT TTTAATTTTA GTTCTCAAAG CATTTAATTT 960
GATGAAATTT TGCCATATTT TTTCTTTATT TTTAAAGCCT GTTATGTTCT ATAAGAAATC 1020
TTTCTACTCA GGATAGTGAA TGTATTCTCT TAATTTTATC TCTCTATGAG TTCCAGCGTT 1080
TTAGTTTTAA TTTTTAAATT GATGACATCT AAAATTCTAC TCCTAACCAA AACATTCCTG 1140
GGGGTGACCA AGGACAACTC CAAAAATCTT CCATAAATGG AAGTAAGACT TACTCCTTGA 1200
AGAACTTACT GGGATCTGGG CCTGCAGGGC ACAGTGGCTT TAGTGCACCT CTGCTCTTAC 1260
GACTATTCAG AAATTGTCTT TGTGAACCCA TCAGGCTGTT TCAAAATCAG CAATTTAGGG 1320
CTTGCTTGCA ACATGCAGTT ATGCAGCAGC TGTTTTGTGG ATCTGGTGAG TGCCTGCACG 1380
CATAGTTCCC CGGGAATTTT CTGAATTTGA ATTCTCATGG TATTTCAAGT GGCTCAGTTG 1440
TCTCTTTCTT TTCTTTTCTT TTCTTTTCTT TTCTTTTTTT TTTTTTGAGT CAGAGTCTTG 1500
CTCTGTCACC CAGGCTGGAG TGCAGTGGCT GGAGTGCAGT GGCGCGATCT CAGATCACTG 1560
CAAGCTCCGC CTCCCGGGTT 1580
|
| |
|
|
|
