| Tag | Content |
|---|
EnhancerAtlas ID | HS044-02659 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr11:94156480-94157460 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr11:94157129-94157140 | AGGGTGTGGCC | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 94156657 | 94157137 | | chr11 | 94157294 | 94157430 |
| Enhancer Sequence | ACCTCAGAGA TCCTAGCTAC AAGATTCCAT GCCCCCTGGA GACGTTTCAA CTGGCAGGGG 60
GATTGGCCCA AACAGTAGGC AGAGACAGAG CTCCAGAATA CATGGAGCCC AGGGGTTTTC 120
ATATCTAAGG CAGCTGCAGC AGAAGGTGGC CATAGGCGCC CATCCCCTAA GACTTCTTAT 180
TTCCCCTGGA GTAGGACTAG CCCCACCTGA ATGCTGGGGC AGGCCAGCCT GGGGCCAGCT 240
TCCCTGTGGG ACAGAGGAAC ATCTGTTCTG CAGGCCCTCC TCCCCTACAG CCCCTTCCAG 300
GGCCCCTGCC AAGCTGCCCT GCAGGAATGT GTGCACAGGG CAGCCTCTGC TGCCTAGCCT 360
TGTTTTTTGC TGGTGGTTCC ACCTGAGTAC CTTCCTGGCA GCCTGGGAGC ATTTCAGATT 420
CCCCAGCACA GCTGGTGCCT GACCCTGAGG GTCCAGACGA TGGAGCCACA GGCTGGTCCC 480
AGTGCTACAG GGCTACAGCA CACAGCTGGG GCTGTCGAGC TAAGAGCTGG GGCTGGCACT 540
CAAGTAGGGG AGAAATCCCA CTTTCAGAAC ACTGAAAGGA GTGAGACACG TGGGTTCGTG 600
GGCCAGTGCA GGAATGGGAC ATGCCTTCCT CCACAGTGCT GGTCTGGGAA GGGTGTGGCC 660
TGTCTGGCAG CCATGGCCTC TGTCTAAGGG AGCCCTGCAA CCCAAGACAC CAAACAACAG 720
TAATGCAGGT ACAGTGCCAG TGATAGGAGG GACCTCACCC ATGGTCCAGG AGTGGCCCTT 780
ATGAGTGGTC ATCTCTCTCC CCAACCCCAC CACAGAGCAC GGCTGTGAAC ACACAGAAAT 840
ACAAAAGAAC TATGCAGCTG AGTAAGAGCC TATCCACTGG ACACTAATGT TAAATGCCAG 900
CTACTGGATC ACAGCCAAAA TTACAACACC AAAATAATTC TGCCAATATA CATCTCTGTG 960
ACACCCAGGG CAAGAATCTA 980
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