| Tag | Content |
|---|
EnhancerAtlas ID | HS044-01249 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:231835260-231836150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:231835660-231835681 | TTTCACTTTCACTTCTTGCTT | + | 6.18 | | IRF1 | MA0050.2 | chr1:231835654-231835675 | TTTTCATTTCACTTTCACTTC | + | 6.75 | | PRDM1 | MA0508.2 | chr1:231835662-231835672 | TCACTTTCAC | + | 6.02 | | ZNF263 | MA0528.1 | chr1:231836023-231836044 | AACCTCTCTTCCTCCTCCTCC | - | 6.46 | | ZNF263 | MA0528.1 | chr1:231836026-231836047 | CTCTCTTCCTCCTCCTCCTCA | - | 8.25 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 231835574 | 231835796 | | chr1 | 231835867 | 231835977 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I231699 | chr1 | 231835347 | 231835946 |
|
Enhancer Sequence | TCCTGTTGGC TCTATATTTA ACCAGCGGTC TTCTGAATAT AACCGGAATC AGATCACATC 60
TCACCATCTT CACCATTGCC ACCATCCTCA CTATCATCCA AGCTCCTGTC ATCTCCTTCC 120
TGAATGTTCC CATAGCCTCT TACCTGGCCT CCCTTCTTCT GCTCTTACTA ACAGCAGCCA 180
GAGTGAAACT GTTTAAAACA TAAGTCAGAT CATGTGCTCC TCTGCCCCAA ACTCTCCAGT 240
GGCGCCCCAT GAACTTCAGA GTAAAATCAG AACTTTTAAA TGGTCTTCAT GTCTCTTCTT 300
GACACAGTCC TCATTACCTG TGTGACCTCA TTCTCTACAG TTTTCCCTTA CATCAATCTG 360
CCCCAGATCC AGTGGCATTC TTGCTCCCTC TTGCTTTTCA TTTCACTTTC ACTTCTTGCT 420
TTCTTACCAG AAACACTTCT GCCTGAGCCT TTGTACTGGC TCTTCCCTCT GTGGGAATAT 480
TTTTCTCCCA GACAGCCTCG TGGTTCACTC CCTTACCACT TTTAAATCTT TGTGTAAATG 540
TCACCATCTC AAGGAGATCA GATTTCAAAT TGCAACCTCT ACCCTCTACC AGCATCCCTG 600
ATCCCCATAA CGTGGTTCTC CCTTTTCCTT TTTCATAGCA TTAATCACTT GCTAAGGTGC 660
CATAAAACTT ACAGTTGACC CTTGAACAAC ACGGGTTTGA GCTGCAAGGG TCACTTATAT 720
GCAGATTCTC TTCCACCTCT GCCACCTCTG AGACAGCAAG AACAACCTCT CTTCCTCCTC 780
CTCCTCAGCC TACTCAAGAT GAAGATGATC CACTTTCACT TAATGAATAG GAAATTTATT 840
TTCTGTTTTT TATGATGTTT TTCGTCATCT AGTCAATGCT GAATTTTTTT 890
|
