| Tag | Content |
|---|
EnhancerAtlas ID | HS105-42003 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:20348430-20349880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| 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 | CACAGAAAAA ATTGTCTTCT GCCTCCAGTG CTCAACTGAG CCATTCAGAT GAAAATATCC 60
CACTAGCCAC ATCGACAGCT TAATCTGGGG CAGGGGAGCT AGACATTAGT AAACCGCCAC 120
TCACTGCCCC CTATACAAAT ACATACTTAC AGACACCCAC TCCTACACAC TCAAAATTCG 180
AAGCTCTGGT ATGTGCTCCA TGATTAGGGC TTTCTTTGGG GTTACAAGGA AGCAGAGTTG 240
TAAATCGGTA TTAGAATGTG ATCAAAAGGA ATGTCTGTAT GCAATTATTT TGTTTTGAGA 300
CCAGTGTTCA GAGGCACCGA CTTTAAAGTG CTGGCTTGGT CACGTGGTGG CCTCTCACAC 360
ACATAGGCGC ATATGATTTT GGTCCCCACA AAAGAAGGAA GACAAAGGCC CGGGTTTTCT 420
CTTTGTTGCT TCTTTGTTTC AGGACGGAGT CTCACCCCAA CAGCTCAAAG CACCCTCTCC 480
CCCATCTCCC CTGGCTGTCC ATTCCCTAAC TGTTACAAGA GGAAGTCTTG CTAATATAAC 540
CTCTTGCCCC GGAAAGTAGC AGTTACTGTA ATTTGAGAAC AGAGATCCCT TGCTTAACAG 600
AAATTCACTT AACAAAACTT CAAATTAAAC AAGAGGTCAG TGAAAGGAAA TAACATTTGT 660
GAGGCATGTC TACTGAGTTC TGGGCAGTGT GCTGGGCAAT TTCACACAGA TTTTTGCATT 720
TCATTCAATG AGTCATCACA ACCACCCCAA AGTGGAGGTA TTATTATCCC CCGTATTATA 780
CCAAAGAATC TGAGGCTCAG AGTGGTTATG TAACTTGCAC ACGGTCACAA GGTTAGGAAG 840
TAGCAAACCA AGTAAAAGAT CTCCTCAAAG CAACATCACA GAGAAAAAAA TGTTGAGGAA 900
TTCGGGTGTC CTATGAGTCC ATCTTGCGGT GGCTGGCTTG CCCAGGCTGC TGCCATCTGT 960
TACACATGCG CATGAGAAAG CAAAACTCAG TCCATCAGAT AACGTCTGAG AGCAGTCAGT 1020
GCTTTGTGAA GCCCAGCAAG CCACCGTTCA CCAGTGGGCA TAAAACCAAA GCTTTATGTT 1080
TCGGAACAGA ACTGTTAATA CAGACGCATT CTAGTGATTG CATTATCGGC ACCCTAAGTC 1140
ACAAGGCTCT GGTCTGGGTC CCTGTTTACC CAGCTTCATT TGTAGTTGCC TTTCCCTTCC 1200
TCTCTGGGCT CCAGCCAAAT AGCACCTGGC TGTCCCTCGG GGCCACCATG TTCCTTCCTG 1260
TCTCAGACCC TTGGCTATTG CTCTCCCTCT AATTGTCCTT CCCAAGGCAT CTCTTCCCAG 1320
CACCACTCAG TAACTTTCAT TAGAAGGAGG CTCCATGGGG CAGAGATTTT GTCTGGCTGG 1380
TTCAACATTG TATCCCCATA GCTGGAACAC AGTTAACACT CAATAAACAA CTGTTGAGAG 1440
GACGAATAAA 1450
|
