| Tag | Content |
|---|
EnhancerAtlas ID | HS044-02855 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:125084100-125085430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:125084675-125084696 | CTCTCTTCTCTCTCCTCCCCA | - | 6.38 | | ZNF263 | MA0528.1 | chr11:125084648-125084669 | CTTCCCTCTCCACCCTCCTCT | - | 6.94 | | ZNF263 | MA0528.1 | chr11:125084672-125084693 | TCTCTCTCTTCTCTCTCCTCC | - | 7.21 |
|
| | 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 |
| GH11I125213 | chr11 | 125083390 | 125086768 |
|
Enhancer Sequence | TGGAAGAGAG CTAGGCTGTC ATCTGAGTGG GCTCCATGAG CGGCCACCTC CCAGCCCCAC 60
CTACCCTTGA ACCTGAAATT CTACCATTCC CAGTTTGTTC CTCAGAGCTG GCATTTCCTC 120
TTCTGATTCG CTCTTGCTCT CCCTCTTACT CCCTTTCTGT CCCCCTCTTT TGAATGCCCT 180
ACTCGGGAGG GGGTTGCTCT GGAGCATGGA TTTGTGTTGT CAGCCTCTTT TCTTCTGGCT 240
AAGAGTGACA GCCAGAGTAA GAGGTCTAAA TCATGTACCT GGGAGGATAG CTGATCCTGA 300
AAAGGGAAAA AAGGAAAGGC TCCTCCACCT AAGACAAATC TTATACCCTT CTGAGTTTTG 360
CCTGGGCTGG CCCTGCCTGG GTGCAAGTTG AGCCATACCC TGGGCCAGCC TCTGAGGTCT 420
GCGTCCTGCT GTCAGCACCC CCTAGTTAGC ATCTGCACCA TCAATCAGGC AATGCAGCCC 480
CTGCCTGAGG GGTGGAGGGG ATGGGGTGCA GCCTCTCCAA CTCCTTGCCA ACCCTTAGAC 540
ACAGAGCCCT TCCCTCTCCA CCCTCCTCTT TTTCTCTCTC TTCTCTCTCC TCCCCACCTT 600
GATGTGGACA GCTCAGCCCC TCCAAGGCTT CTGTCCACTC CGAGAACCCC TCTCTATCCA 660
TAGTGGCTCA AAGGGCTTTT TGAGTGGGGA AGCAGGCAGC CTGTGGGCCT GGGAGGAGAG 720
ATAAAGGCGT GAGATCCCCC AGGGGCCTGC GGGGTCAGGG GCTGTGTATC TGGTGACTTC 780
TGAATGCAAG CTCCAACAAA GAGAAATCTG TGGTGGGAGA GCGTCCGCGA AGGAAATAAA 840
ATCTCCATGA AAACAAACTT TTGTTGGAAG CTTTCTCCTC TTGTTTTGGC AGCGTTGCTA 900
GGTCCTGGGA GGGGAAGGCC GTGTCTTCCG GAGCAGTTGG GAGGCTCTCG GATTGTCCAA 960
ATATCAGCTT GCTGCAAGAA GGCTGTTCTT CCCCCACCAG GAAGACGGGG CTTAGGAGTT 1020
AGTGCAGTAA TCATTGGTTT TCTAATCAAG GCTAGAATGG CTGAAAGAAA GGCTGGGGGC 1080
CATGGAGAGG GCTCAGGACT GTGAGTTAGG AGAATCAGCA CTGTGTGTGT CACAGTTCCG 1140
TGACTCAGGC CAACCTGAGA TCCCTTCGTG CCTTACTTTT CTCACCTGTA AAACGAGCAT 1200
AACTTGCCCA AGGTCATTCA GCTAGAAAAG CAGGAGCAGG CCCAGGATAT AAACTGCTAT 1260
TTCCATGCTG GGCGCGGTGG CTCATGCCTG CAATCTCAGC ACTTTGGGAG GCTGAAGCAG 1320
GCGGATCACC 1330
|
