| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06854 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:20348300-20349660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr2:20348426-20348437 | AAACCACAGAA | - | 6.32 | | USF1 | MA0093.2 | chr2:20348767-20348778 | GGTCACGTGGT | - | 6.32 | | USF2 | MA0526.2 | chr2:20348764-20348780 | CTTGGTCACGTGGTGG | + | 6.05 |
|
| | 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 |
| GH02I020148 | chr2 | 20348200 | 20349900 |
|
Enhancer Sequence | ACTTTGTTTT TAGTCTGCTT CTTATTAAAA ACAGACTGGG ACCCAAAGAA ACCCCATCGG 60
GGTAGGTAAT GAAGTAATCA TGATCATACT AAAAGAACAG AATGGAAAAA CTGCCTGGCC 120
TGGAGCAAAC CACAGAAAAA ATTGTCTTCT GCCTCCAGTG CTCAACTGAG CCATTCAGAT 180
GAAAATATCC CACTAGCCAC ATCGACAGCT TAATCTGGGG CAGGGGAGCT AGACATTAGT 240
AAACCGCCAC TCACTGCCCC CTATACAAAT ACATACTTAC AGACACCCAC TCCTACACAC 300
TCAAAATTCG AAGCTCTGGT ATGTGCTCCA TGATTAGGGC TTTCTTTGGG GTTACAAGGA 360
AGCAGAGTTG TAAATCGGTA TTAGAATGTG ATCAAAAGGA ATGTCTGTAT GCAATTATTT 420
TGTTTTGAGA CCAGTGTTCA GAGGCACCGA CTTTAAAGTG CTGGCTTGGT CACGTGGTGG 480
CCTCTCACAC ACATAGGCGC ATATGATTTT GGTCCCCACA AAAGAAGGAA GACAAAGGCC 540
CGGGTTTTCT CTTTGTTGCT TCTTTGTTTC AGGACGGAGT CTCACCCCAA CAGCTCAAAG 600
CACCCTCTCC CCCATCTCCC CTGGCTGTCC ATTCCCTAAC TGTTACAAGA GGAAGTCTTG 660
CTAATATAAC CTCTTGCCCC GGAAAGTAGC AGTTACTGTA ATTTGAGAAC AGAGATCCCT 720
TGCTTAACAG AAATTCACTT AACAAAACTT CAAATTAAAC AAGAGGTCAG TGAAAGGAAA 780
TAACATTTGT GAGGCATGTC TACTGAGTTC TGGGCAGTGT GCTGGGCAAT TTCACACAGA 840
TTTTTGCATT TCATTCAATG AGTCATCACA ACCACCCCAA AGTGGAGGTA TTATTATCCC 900
CCGTATTATA CCAAAGAATC TGAGGCTCAG AGTGGTTATG TAACTTGCAC ACGGTCACAA 960
GGTTAGGAAG TAGCAAACCA AGTAAAAGAT CTCCTCAAAG CAACATCACA GAGAAAAAAA 1020
TGTTGAGGAA TTCGGGTGTC CTATGAGTCC ATCTTGCGGT GGCTGGCTTG CCCAGGCTGC 1080
TGCCATCTGT TACACATGCG CATGAGAAAG CAAAACTCAG TCCATCAGAT AACGTCTGAG 1140
AGCAGTCAGT GCTTTGTGAA GCCCAGCAAG CCACCGTTCA CCAGTGGGCA TAAAACCAAA 1200
GCTTTATGTT TCGGAACAGA ACTGTTAATA CAGACGCATT CTAGTGATTG CATTATCGGC 1260
ACCCTAAGTC ACAAGGCTCT GGTCTGGGTC CCTGTTTACC CAGCTTCATT TGTAGTTGCC 1320
TTTCCCTTCC TCTCTGGGCT CCAGCCAAAT AGCACCTGGC 1360
|
