| Tag | Content |
|---|
EnhancerAtlas ID | HS073-11316 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr5:251680-253070 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PPARG | MA0066.1 | chr5:251750-251770 | CTGGATCACTGTGACCTTTT | + | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 252134 | 252201 | | chr5 | 252318 | 252385 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I000251 | chr5 | 251974 | 253253 |
|
Enhancer Sequence | CCCCAAAAGT AAATCCAAAA AATGCCTTTT TCCCCCCTGG TAACTTTGAT CCCTGGGTTC 60
TCGCCATCTT CTGGATCACT GTGACCTTTT CCTTGCTTTG GGTCGGCATC CACTGATGCC 120
AGCAGTGGCA TCTCCAAGCC AATGTGCTTT GCTGTTAGAA GGCCAAGGTT AGAAGTGCAG 180
CTAGAGTGGC AAGACCAGGA AATAAATGCC AGTTTATTAA ATAACGAGTA AGCCATCATT 240
TCAAGCCTGC CCTGTGGAGG AAATGCCAGT TTATTAAATA ACGAGTAAGC CACCGTTTCA 300
AACCTGCCCT GTGGAGGAAA TGCCAGTTTA TTAAATAACG AGTAAGCCAC CGTTTCAAAC 360
CTGCCCTGTG GAGGAAATGC CAGTTTATTA AATAACGAGT AAGCCACCGT TTCAAGCCTG 420
CCCTGTGGAG GAAATGCCAG TTTATTAAAT AACGAGTAAG CCACCGTTTC AGACCTGCCC 480
TGTGGTGGAA ATGCCAGTTT ATTAAATAAC GAGTAAGCCA CTGTTTCAAA CCTGCCCTGT 540
GGAGGAAATG CCAGTTTATT AACGAGTAAG TCACTGTTTC AAACCTGTCC TGTGGAGGAA 600
ATGCCAGTTT ATTAACGAAT AAGCCACCGT TTCAAACCTG CCCTGTGAAG GAAATGCCAG 660
TTTATTAAAT AAGGAGTAAG CCACCGTTTC AAGCCTGCCC TGTGGAGGAA ATGCCCGTTT 720
ATTAAATAAC GAGTAAGCCA CCGTTTCAAG CCTGCCCTGT GGAGGAAATG CCCGTTTATT 780
AAATAAGGAG TAAGCCACCA TTTCAAGCCT GCCCTGTGGA GGAAATGCCA GTTTATTAAA 840
TAACGAGTAA GCCACCGTTT CAAGCCTGCC CTGTGGAGGA AATGCCAGTT TATTAAATAA 900
CGAGTAAGCC ACCATTTCAA ACCTGCCCTG TGGAGGAAAT GCCAGTTTAT TAACGAGTAA 960
GTCACCGTTT CAAACCTGCC CTGTGGAGGA AATGCCAGTT TAGTAACGAG TAAGTCACCG 1020
TTTTAAGCCT GTCCTGTGGA GGAAATGCCA GTTTATTAAC GAGTAAGCCA CCGTTTCAAA 1080
CCTGCCCTGT GGAGGAAGTG CCAGTTTATT AAATAATGAG TAAGTCACCG TTTCAAGCCT 1140
GCCCTGTGGA GGAAATGCCA GTTTATTAAA TAACGAGTAA GTCACCGTTT CATACCTGCC 1200
CTGTGGAGGA AATGCCAGTT TATTAACGAG TAAGCCACCG TTTCAGACCT GCCCTGTGGA 1260
GGAAAATGCC AGTTTATTAA CAAGTAAGTC ACTGTTTCAG ACCTGCCCTG TGGATGAAAT 1320
GCCAGTTTAT TAATGAGTAA GTCACCATTT CAGACCTGCG CTGTGGAGGA AATGCCAGTT 1380
TATTAAATAA 1390
|
