| Tag | Content |
|---|
EnhancerAtlas ID | HS041-12073 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr2:172877930-172879370 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid5a | MA0602.1 | chr2:172878438-172878452 | TATGTCAATATTAG | - | 6.18 | | IRF1 | MA0050.2 | chr2:172878714-172878735 | TTATACTTTTTTTTTCTTTTT | + | 6.13 | | IRF1 | MA0050.2 | chr2:172878372-172878393 | AAGATGAAAGTGAGAGCGAAG | - | 6.32 | | PPARG | MA0066.1 | chr2:172878022-172878042 | CTAGGTCAGTATGTCCAACT | + | 6.25 |
|
| | 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 |
| GH02I172013 | chr2 | 172878061 | 172878210 |
|
Enhancer Sequence | AGAAAAATCA GTAACTCTTA ACAGGGGATT TAGCCTAGTT TACAAGAGTA TATGATCTGT 60
GCAGCAGACC TTGAACACAG CTAATTGCTT GTCTAGGTCA GTATGTCCAA CTGGCAACTC 120
TCAGAGCCCA TCCAGGCCAC AGAGCATTTC CGGGTGGCTT GTGTGTGCGC TCCGGCTGTC 180
GAGCAGCAGG ACTTGGCTTC TGTTCCCGGC TTCGTTGGCC CCATCTTTTA GTTCAGGTCC 240
ACCCCCTCCT GCCTCAGAGG CCTGGGAAAC CCAGCCTGGC CACCTGGTGT CCTCATGCCC 300
AGCATCTACG CATCTGCCCC AGTTGTCCCC TCAGCCACCT TGGCAGATTT CTTGACTTAA 360
CAGTTCTTCC CTGAACTAGG ACCGGGGGCA GGAGTTATTA GAGAAGGGAG AGGAAAGGTG 420
ACAGGTCTCA GGAGTCTGAG GGAAGATGAA AGTGAGAGCG AAGTAGTGTG GGAGAGAGGG 480
GGATCACATC CATGGGAGAG AAAATAAATA TGTCAATATT AGGGTGGTGA GGCCTGTATA 540
CAAAGACAGG ATGGCAGGGA GAAGAAGTAG GCAAGGACAT AAAGGGGCTT GGGTATGCAG 600
ATGCTGGTCA CTGAAATGAG GAACAAAGGA GGGAAATTTG CGTGTGAAAG AGGCCACATG 660
TGAGAGAATA GAGAGAGCAA AATGACAGCT TTGCTTGGCA GAACGTGACC ATGCACAGCA 720
TTGGGAGACA CAGTCTGATG AAGCATTTTT TCCAATTTGT AAATATATTT ATAACAAAGA 780
AACATTATAC TTTTTTTTTC TTTTTTTTTT TTTGAGACAG AGTCTTGCTC TGTCACCCAG 840
GCTGGAGTGC AGTGGCGTGA TCTTGGCTCA GGGCAACCTC CGCCTCCTGG GTTCAAGCGA 900
TTCTCCTGGC TCAGCTTCCC GAGTAGCTGG GACTGCAGGT GCGCACCACC ATGCCCAGCT 960
AATTTTTTGT ATTTTTTAGT AGAGACGGGG TTTCACCATA TTGGCCAGGC TGATCTCGAA 1020
CTCCTGACCT CAAGTGATCT GCCTGCCTCG GCCTCTGAAA GTGCTGGGAT TACAGGCGTG 1080
AGCCACTGCA TCTGGACTAC TTTTTTTTTT GAGAGGGAAT CTCACTCTGT CACCCAGGCT 1140
GGAGTGCAGT AGCAGGATCA CTGCAACCTC CACCTCCTGG GTGCAAGCGA TTCTCCTGCC 1200
TCAGCCTTCC CAAGTAGCTG GGATTACAGG CACCTGCCAC CATGCCTGGC TAATTTTTGT 1260
ATTTTTAATA GAGACAGGGT TTCACTATGT TGGCCAGGCT GGTCTTGCAC TCTTGACCTC 1320
AGGTGATTTG CCTGCTTCAG CCTCCCAAAG TGCTGGGATT ACAGGCATGA GCCACCGTGC 1380
CTGGTCAGAA ATTTATTATT ATAAAAACAC AAAGAGATAT ATACTTAGCA TATTACATTA 1440
|
