Tag | Content |
---|
EnhancerAtlas ID | HS188-11432 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr6:150048700-150050940 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr6:150049483-150049501 | GGGAGGAAGGAAGTAAAA | + | 6.33 |
| | 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 |
GH06I149727 | chr6 | 150048834 | 150051843 |
| Enhancer Sequence | AATATAAACT CTTGGGTAAT AACAAAATAA AATGATCATG AGAAAGAATT TCTAGACATA 60 TTTCTAGATG AACATTTCTA GAAATATATT TCTAAATATA TATTTGTTAC TATATTTCTT 120 AAAATATAAT CGCCTTACCT CAAATCTTTC ATTCTTATGC TTTTTAGATA AATGTTCTTA 180 CAAGCAGATT AGAACACTAC TAGATTATAA GGTTTTATCT CTAACAGCGC ACTGTACTTA 240 CTATAGAATA AAGTGAGGCA GAGGCAGTAT ATTTCAATTT TAGTCATTAT TCGCAACTTA 300 CTTTCCTCTC AACTTGCTGT CATATCAAAT AAGTACAAAT TTAATTCACT CAACAAATGA 360 CTGAGTACCT ACTATGTGCC AGGCTCTGTG CTAAGTGCTC TGTGCCAAGT CCCTATGTCT 420 TGAAGCTTAA AGATTAGTAC ATTTAAAATC TTGCTGATCC TTTAAAATAT GGCTGAACTT 480 CCTTCTCTAA GAAAACTTTG AAGACAACCT CTACTTCATG TTTTTCTCTT TCCTTGAACC 540 CTCAGCACTT GTATGTACCA TTAATTTACT ACTTTATAAC AATTCTTATA TCCTAATTGA 600 ACTATCCATG CCTCTGTCCA TGACTAAATA TGTCTTAAGA GCAGGATGCA TATTTTATAT 660 GTTTTACTTT TTCACAGTGT CTAATACTGT GCCTTGCAAT AGTAGACACA GAATAAAGTT 720 TTATTTCCAG TCTAACCAAG GTTCCTTAAA AGTAAACTTG CAAGTTCAAG ACTGTGCGGT 780 TAGGGGAGGA AGGAAGTAAA AACGAAGTAC ATACTTAGTT AATCCTTAGA TGAAACTGTT 840 TGTTTCTCTG TAGATGAAGT TATAGCATGG ACATGCATGC ATGCTCCACA CATGCTCTCC 900 GCTCCAGAAT TTTTCTGAAG AAGTTTTAGA ATTTTTTTCC CCTTAGTTTT TCTGTTTATC 960 TTTTACTGCC CCTACATTTT ACATTGCTCT TGGACGCTGT AAAGATTAAC ACATTATTCA 1020 AGCCACTGTG ATAAGACTCC TTCCTCATCT CCCTGTTTTC CACTTTTCTC CTCCCCCTCC 1080 CATAAGTCTA AAGTCCTTAT CATGGGCTAC AAAGTCCCAG GGCTCCTCAG CCACCAGTCC 1140 TTATCTCCCA CCACTGTACC CTGCTGCCTG AGCTCCAACC GTGGTGTCCT TGCAGTTCTC 1200 TGCCTGTCTC AGGCCCTCAG CATTTGCTGT TTCCTCTGCC TGGAATGCTT TCATGTCACT 1260 TATGCCTTCA CTTCTCTTAA GTCTCTGCTC AAATGTTCCT TCTGCCAAGT GGCCTCTTCT 1320 GACTCTCACT AGAGTAGCTC CCCTCACCCC TGTCTTTATT CTTTATCCTC CTACTCTGCT 1380 GTATTCTTCT TCATGGTAAT TAGCAGTGTA TTTGGCCATG TTATTTTCCT TTTTCTTTTT 1440 TTTTGAGATG GAGTCTTGCT CTGTTGCCCA GGCTGGAGTG CAGTGGCGTG ACCTTGGCTC 1500 ACTGCAACCT CCAACTCCCG GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC AGAGTAGCTG 1560 GGATTACAGG CACCCACCAC CACGTTCAGC TAATTTTTGT ATTTTTAGTA GACACAGGGT 1620 TTCACCATGT TGGACCAGGC TGGTCTTGAA CTCCTGGCCT CAGGTCATCT GCCCACCTCG 1680 GCCTCCCAAA TTGCTGGGAT TACAGGTGTG AGCCACCGCG CCCGGCCTCC TTTTCCACTT 1740 TGCTGTGCTC CACTATATAC TGTAGGAGGT AGAAGTTGGT AAACTCCACT TTCCAGGCTG 1800 CTTTGCCATC TGCCATCCAG ATGGGCCTTG CCAATAGCAG GTATTAATGG TGGGTGACTG 1860 GAAGGCGGAA GGGAGAAGCA GCTCCTTCCT GCTCCAGGTT TCTGGCAACA ACACTGGTGG 1920 TAGTTTCAGC CTGGTTGAGG GAGCGCCTTT TCTCCTAATT CAGAACAAAC TTTTACAGCA 1980 TTTTCAACAG TCAAGTAGCA GGGGTACTAA CAATTACTAT TTCTGGGTTT TCCCTTTTCT 2040 TCCTATTTGT TCTCCCAGCA CCCCTCCTAT TACCTTTTGT TTTCCCAGCC CTTCTAACAC 2100 ATGTGAGACC AATTCCTTCT ACATCTAAGG TAGTTTCTGA CATTCTAATT GGACTCTTAC 2160 TGATACATTA TCTATTTTTT TAACTATTAG AATATTTGCT CTATGCGTTT CGACATTTCG 2220 TTCTGCTCAC TGTTACACGT 2240
|
| |
|
|
|