| Tag | Content |
|---|
EnhancerAtlas ID | HS091-41415 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr6:52824500-52826800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr6:52825965-52825980 | AGGGGGCAAGGGTCA | + | 6.39 | | STAT1 | MA0137.3 | chr6:52826201-52826212 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr6:52826201-52826212 | TTTCCCAGAAA | - | 6.32 | | Stat4 | MA0518.1 | chr6:52826198-52826212 | CCCTTTCCCAGAAA | - | 6.56 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGACATCTCT CCAAGTGAGG TCGAAGGTTT GCCCTAGACC TTGTAGGACA TCTCTGTACC 60
TATCAGGATC ATCTGAAAAC TTCCCCAGGT CTGCCTTGAT CTGTTTTAAG TCAGAGAGGG 120
AGAAGGGGAC ATGTACCCGG GTTGGGCCAA ATTCCCCTCC CCCTACAGCT TGAAGGGGAC 180
ATAACCAGTA GCCTGGGGGC ATTTGTGGTC CTTTGGAGAT TTCTTTACTT ATTTCCTTCT 240
GGGCAGGGGA GATTAGAGGA GGATTATCAT TAATGGGAAG GGGAGCTATA GGGAGGCTAT 300
GATATGGGGG TAAGTTGAGC GGTCCTCCTG TGGGATGTAA ATTGTAAGCT TTGCATTGTT 360
GTGTATTCTC TGTCAATGAA AAGAAAGCTT GGACATAAGG TATTTCACTC CATTTGCCTT 420
CCCTCTTACA GAAAAGGTCA AACTGCAGGA TAGTATTGTA ATTTGTACTT CCCTTCAGGT 480
GGCCATTTTT CCCCATCAGA GAGAGAATAT TGGGGCCAGG CTGTAGTGTA GAAAAAAATG 540
AGCCACCTCT TTTTCGGGGT TTGTGGGTCA AATTGGTCCC AATGGCTTAG GATGCATTTC 600
AAGGGTGAAC CTGTTGATGC CTGAGTGTTT CCCATCTGAA AGACAAAACT GCCTGCGGTT 660
TTGGTTTGTT TTGTTTCTCC CCCTGCCCAA GAACCCGTGA CAGTCCCTGA ACCCTGCTGA 720
TCGGAATAGT TGTGCTCACT GATGCAGCAA CAGAAACAAC CCCTACCCAA GAACCCGCAA 780
TGGTCCCTGG ACCCTGCTGA TCAGAACAGT TGCGCTCACT GACGCAGCAG CAGAAACATT 840
AATTTTCCTC CCAGACCACA TGGAGGACCA AGGAAGGTCG GATTTAGTGG CCCTTACTGA 900
TGCATTCTCG AAAACCTGCA CCCTTGCCTG TCCTCCTAGA CCACAAGGAG GGCTGAGAAA 960
AATCGGATTT AGTGACACTT ACCAACGCAT TCTTGAAAAC CTGTTAGAGT CCTAAGCATT 1020
CACCTGTTAG TATTGGGACC TTACCCATGT CCTATAAAGA TGTTATGCCC CAAAAATGAA 1080
GTGGAGGGCC ATACCCTGAG GGAGGGAAGG GATCTCCAGG GTTGGAATAG TGACACCTTT 1140
TGTCCTCACT TATATGAATA GGAAGGATAC AATTTCTGGG GCTCCCCATA TCCTAGCTTC 1200
AGGAATAGCT TTTGTTAGGC CTGTTAGTCT GAGGAGGGAT CCTAAAATTC CAGGTAGTCC 1260
CCCCTACAAC AGGGCTTTGG GCAATAATTA TGTCTTTCTG ATTGGTGAGC CAGGGTGCCT 1320
AAAGAAGTTA ACAGAGTCTT GGAGTTTATA CTAGAAGTCA TTCTTATAGG AGAAACTAGA 1380
AAAGCCCCAG AGACAGGGAG CGATTTTTAG AAGTGGGACT AATCTCGGAG AAGAGAGGAA 1440
GTTTGTCTGG CAGGCATTAG GACCCAGGGG GCAAGGGTCA GGATAGACAG GATAGATGGG 1500
CGAGTCTCGC TTAGGTGACA CGCCTTTGAG AGTTCCGCTC ATGACCGCAG GGTCAGCCAA 1560
CTTGTTGTCA GGACCCCGGA GCTGAATGGC TTTCCTCTCT CTTGACTCTC AGCTCAGCCC 1620
AGAAGTACAG GAAAAGCAGA AGCCGGTTCC AGGCAAACCA ACGCTCCCAA CTCTGAAGAG 1680
TCAGGGGTTG TTAGAGAGCC CTTTCCCAGA AAGCCTGACA CCTGTGTCTT TAGGCCGGCG 1740
GCCGCGCTAG TCACCTTTAA CTGGCCAACA GGTGCCCGGT ATTTAGCCCC CAAATTCTAA 1800
GGAAAAATAG GACAGAATAG CAAGCAAAAG GGGTCCAATG GTACTCACTG CTTGCCAATA 1860
GGTGACAGTC TTACCGCTTA ACAATAGGCA ATGGTCTCAC CACTTGGTGA TAGTCTTACT 1920
GCTTGGTGAT AGGCAATAAT CCCTTCTGGG TCACCAAAAT GTGTCCGGAA TTGGTGGGTT 1980
CTTGGTCTCA CTGACTTCAA GAATGAAGCC ACAGACACCT GCAGTGAGCG TTACAGTTCT 2040
TAAAGATGGC GTGTCTGGAG TTTGTTCCTT CTGATATTTG GACGTGTTTG GAGTTTGTTC 2100
CTTCTGGTGG GCTCATGGTC TCGCTGGCTT CAGGAGTGAA GCTGCAGACC TTCGTGGTGA 2160
GTGTTACAGC TCTTAAGGCA GCACGTCTGG AGTTGTTCGT TCCTCCTGTC TGGAGTTGTT 2220
CATTTCTCCT GGTGGGGTCG TGGTCTCGCT GGCCTCAGGA GTGAAGCTGC AGGCCTTCAC 2280
AGTGAGTGTT ACAGCTCATA 2300
|
| |
|
|
|
