| Tag | Content |
|---|
EnhancerAtlas ID | HS059-26175 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr2:112663300-112664740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:112663478-112663499 | AGAAGGAAAGAGAAAGAGAGA | - | 6.4 | | PRDM1 | MA0508.2 | chr2:112664023-112664033 | TCACTTTCAC | + | 6.02 | | ZNF263 | MA0528.1 | chr2:112663467-112663488 | GGAGAAGGGGCAGAAGGAAAG | + | 6.26 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 112663535 | 112664666 | | chr2 | 112664507 | 112664640 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I111906 | chr2 | 112663778 | 112664577 |
|
Enhancer Sequence | CTCCCAAAGT GCTGGGATTA TAGGCGTGAG CCACCGTGCC CAGCCAGAAA CCTACACTCA 60
ATTCTAAAGC ATTTTATTTC ATCCTTCTTG GCTAGTTCTT CAATTATCAG TGCTTCTTTC 120
ACTCAATGGT AAATGGATTT TCCATGAGTC TTGGAGGTGG CAGGCAGGGA GAAGGGGCAG 180
AAGGAAAGAG AAAGAGAGAA CAGATGTTGG CTTTATGTTT GGAATAAAAT TACACCAAAA 240
GCTAAGAACA TTTATATTTG TGCTTAGAGA AACCCCATTT CATTTCAGAA GCTCAATGCC 300
TGGATTTTTT TGCCAGCACA TTTTACACTT GTATGTTTCT CCTTGTACTC TGTGCCTCCA 360
TGTATTTCTG TTGGTCCCTT GAAAACAAGA TCCAATCATC ACAGGGTTAG TGCTCTGCCC 420
TAGGTCACTC CAGTAGGGGT CCATCCTCCG GATTTAGATC TCAGGTTGGC ACTTATGCAA 480
ATGCTTTCTG ACAGGTCCCC TTTTTTGTGT AATCTGCTTT TTCTTTGAGG ATCTAGATAC 540
CTCAGCATTC AGGGACAGTA AACATCTTAG AACTTGCCTT AGCTGTGGTC TTGCCTCTCA 600
TTAGATACAC AAAGAAAAGC CTTGTTTATT TTGGAGAAGG AATTGTTTTG TTATTTTAAG 660
CCTTAGGGCC TTGTGGTTAG AGCTACCAAT AGTAGATTGG CTTCATTATG GTTTTGAAAA 720
TGATCACTTT CACAAGTAAG AACAGGCTGT CTTAGTGGAG AATATTAGAA CAGAGACTCA 780
AACTTAACTG AAAGTTGTTT TCTGTCACTG TGCCGCTTAG GGAATTCTCA GTGCGGTGAT 840
AAATATTCAT GGACTTCCCA AGTGTTGTGT GTGCCTGGAG GCCAGTTTTT CACTTGTTCC 900
AATTAACGGC AGGCTGCCTC CACACAGGAA GTGAAACCAG CCTTTAAGCC TTTTTACAAT 960
TCTGGCACAT GATTTGAAGA TTTGGTGATG AAAGCAATGT TCTTTGAAAG TTTTGGAGCA 1020
AATAAAAAAA AGAAGCTTTT TAGATTCACT CTTAGTTTAA AAAATAACCA CTTGGGGAGT 1080
TGAAAGATGT AAGTTCTCAT CCTAGCTTTG AGAGGAACCT GCAGGGACAG CTGGGGTATA 1140
GTGTGTCCTC CTTCTAAAAC TCCACATCCT CACTTGTCAA ATGGGAAAGC AGATGGATGA 1200
TTCTAGGCCC CTTTGGGGCA GAACACTGAT TCCATCTAAA GGGGAGAGGT GGGAAGGGAT 1260
ACTTTCTCCC ATGCCGTTTG GGACACAGAG CCTCAGCCTG AGTTTGACCC TCAGCCCTGT 1320
GCGTGACTCT CGGTGTGAAC TTTCTTAGAC ATCAGCCCAG AAACGGAGAT GGAGGCTGTG 1380
TGAAGAGTTT CATTAAAAAT GAGTGATGCA GCCAGGTGCG GTGGCTCACG CCTGTAATCC 1440
|
