| Tag | Content |
|---|
EnhancerAtlas ID | HS105-59508 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr4:4783330-4784520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:4783564-4783582 | GGGAGGCAGGAAGGAAGG | + | 7.88 | | EWSR1-FLI1 | MA0149.1 | chr4:4783568-4783586 | GGCAGGAAGGAAGGAGGG | + | 8.01 | | MAFF | MA0495.3 | chr4:4784287-4784302 | GTGCTGACACAGCAT | + | 6.43 | | MAFF | MA0495.3 | chr4:4784287-4784302 | GTGCTGACACAGCAT | - | 6.45 | | ZNF263 | MA0528.1 | chr4:4783565-4783586 | GGAGGCAGGAAGGAAGGAGGG | + | 6.02 |
|
| | 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 |
| GH04I004781 | chr4 | 4783097 | 4784761 |
|
Enhancer Sequence | TATAAAGCGT AACAGTAGCT TAAGCGATAA AGATGGACTC CTCTTCCACG AGGAGAAGTG 60
GCAGATGGCA GTTCAGGACT GGGGCAACAG CTGAGCATTG GCATCATGGA ACCAGGCTAT 120
TTCCAGCTTT CTCTTCTGTC ATACTCCACC AGATGGCTTT TTGTCCTAAT GGTTGTTGCT 180
TTATGGTCAC AAATGGCTGC TACAGCTCCA GGCATCACAA CCAAGTTCAA AGGCGGGAGG 240
CAGGAAGGAA GGAGGGGGTG GCGAGTTTCC TGAAGTGCTT TCTTCTTATA TCAGCAAAGG 300
AAAAAGGGAA CCAGAGGCAG CTGTCTCAGA AGACTTTCCT TTAAGCCTTG CTTGTTAGTT 360
TGGCCACATG GCCAATCCTG GCTGCAAGGG CGGCTGGAGA AGTGGACCTC CAGCAAAGAT 420
GGACGGGATG GCCAGAGTCG CCCAGGCCAA TCATGATTGT TCCACAGGAA CAGGCTCACT 480
GCTGCTCTGA ACAAAATTGG GGCCAGATGG TGAGGGGAAG GGAAAGGGGT TGCTCCCTTC 540
GAGTTTCAAT TACATGCCAG TAACATTGCT CAGCAGATAT GATTATTTCC TTTTCATAGA 600
TGAGAAAACC AGGGCTCACA GAAGCTGTGA CTCGCCCCCT CGGCTGCCCA GCTTGCGTGT 660
GGTAGAGCCG GAGTCCACCC CTGGCCTGGG TAACTGCAGT GCTGCACTCG CTGCTGTTTG 720
GGGGTCAGTC ACATGAAACA TTCATGAATC ACAATGATTT TGCAGCCGAA AGGGAAGGGA 780
AAGGGGGTAT GGAAGCCCTG ACCACACCGT CATTTAACAA TCCAGGAGAC CAAATCCAGT 840
GTGACTGCCC AAGGACGGGA TCTGGAGGAG ATCTAGCTTT GTACTGATTT TTGGAAGCAA 900
TCTCAGTGGG CAGGGTTCCT AGAAGGCGCC CCACATGAGA GTGTTGATGT TCTCTGCGTG 960
CTGACACAGC ATTCTGCAGC CAAGCAGGAA GGGAGAGTCC CCTCATTCAG TCTGCTTTCA 1020
GTTCTTCAGA TCACATCTTG GAGAAATGAT CAGTAAGTGC AATGAGTGAT CCTTGATGAT 1080
TGCTGGAATT TGCAAAGAAA AAGGATCTAA AGAGTATGAT TGGGTTAACT GGGAGGAAAT 1140
TTGAATGTAG ATTAAGAAGT ACATGATAGA ATTGAATGGA TTTTAAATTT 1190
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