| Tag | Content |
|---|
EnhancerAtlas ID | HS060-00294 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr1:11394390-11396200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:11394682-11394703 | GGAGGAGGAGGAGAAGCAGAG | + | 6.09 | | ZNF263 | MA0528.1 | chr1:11394688-11394709 | GGAGGAGAAGCAGAGAGAGAA | + | 6.34 | | ZNF263 | MA0528.1 | chr1:11394685-11394706 | GGAGGAGGAGAAGCAGAGAGA | + | 7.59 | | ZNF263 | MA0528.1 | chr1:11394679-11394700 | GGAGGAGGAGGAGGAGAAGCA | + | 8.25 | | ZNF263 | MA0528.1 | chr1:11394676-11394697 | GAGGGAGGAGGAGGAGGAGAA | + | 8.88 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 11394600 | 11394756 | | chr1 | 11395791 | 11395892 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I011336 | chr1 | 11395581 | 11395750 | | GH01I011335 | chr1 | 11395761 | 11395910 |
|
Enhancer Sequence | AAAAATTTGG CCTGGTTTGT AAATGGGTCT CTGTCTGCTC TGCAGCCCTC CCTGTGGACA 60
ACTCCTCCGT GCGTGGAGGC TTCTTCCCCG GCTGGGTGGA CCCTACAGGC AGCCAGAGGG 120
ATGTCCCCCT TACCCCTCCC CTTGTCTGGG CCAGCCCCAA ACAGAGGCCG TGGCTGAGAG 180
GGAAGTGTCT GCACCCTGGG GCTGGGGAGG ATGAACTTTG TCCAAACTCC TCTGACTCCT 240
TTCTCCGAGG GTGGTTATTG GGAAACAGGA GTGAAGGTGA GTATGGGAGG GAGGAGGAGG 300
AGGAGAAGCA GAGAGAGAAC AGAGATGGTG TAGGCTGCTT GGTGGCAGAC CGGGGCGTGG 360
GCAGGAAGGC CCAATCTGGT CCCACCAGAT ACCTGGCTTT GCCCTTGTCC TGGGGCAGGC 420
AGGGGGCATT GAGGAGCTGG CAGAACTGTG GACAGAAGGA GAGCGGAGCC GCTTTCTCTC 480
CCAGCGAGAA AAGAGCCCAG TCACTCTCAT TTTCAGGGGA AGCAACATGC CACACCCCCC 540
GAGACACCTC TGTCCCCAGC ACAGTAGCTC CTGATGGCTG CCCGGTGAGG ATGCTGCGGG 600
CAGGTCCCAC TGTCCCCCCA GGCTCTGGCG TGCTCCCCCC AACCAAGATG CCCCAGCAGG 660
GCCCCTAGTG GCCCAGGTCT GTGGCCATCC TGGTTCCTGT CTCCACTGTC TATCTGGAGC 720
CCCTCTCCAA GCCTCCATCC CCCACCAGCC CCCTCCCCGC CTCACCGGGC CACAGCCCCA 780
GCTTGGTCTC TATCTTCTCA CCCAGCCCTG CCTCTCACTA GGCCTCACTG CCGCCTAGCC 840
CTATCCCTTC TTTGGGCCCT GATCCTCTGT CCTGAGTCCT CTGGCCCCGG ACACGTTATA 900
CTTCCATGAC CAAGGGTCTT TGTAAATTCT TCAGGCGCTC TCCAGAAGCC CCAGTCCCCT 960
CATACTCACA GCTCTGAACA CAGCCCGGCC CTGTCCCTAA AACCCAGACA GGACCCGCAT 1020
GTGCCGTGAC CTCCCACTCT CCAGTGTGGC CCCTAAGAAC TCAGGGTCGG GCTTGGCATT 1080
AGCCTGGAGG CCTGGAGCCT GCTCATTCAG TCCTGAGCTG ACAGAGAAGG TCATTAGCAA 1140
GTTCCTAACT GGGCCACACC TCCTGGGCTG TGAGGACGGC TTGTGCCAGA GAAACATCAC 1200
ACTCCGTGTA TCTCACTTCT TGGGGTGGTG GCACTTGGTG GTGCCGGGGA CTCCCACATG 1260
TACTTGTGAG AAGTCTCAGT TCCCCATCTC CTTCTAGCCA CCTCTCTGTC ACCTCCCTCT 1320
GCTGGGTTGT GGAGGGGTGG GGTATGTCTC GGGGTGTCCC TGTGTGGCCT CAGGCATCAT 1380
TTGTAGCTCT CCTGTGGGTT GAGGTTTCTT CTCGGGGCTC ATTCACCCCG GCTCCCATAA 1440
CCCTACCCCA CCATTTCCTA AGCAATAACC CCGTATCAAG CACTGGGCTA AGCAGGATCT 1500
TCATGGCCTC ACAAGGTGGG ACCTGTCACT ATTTCTGTGC TCAGCAGAGG AAATGGAGGT 1560
TCAGAGTTGT CAAGCCACTT GCCTAAGGTC ACAGAGCTAA ACCCTGGTGG AGCTGTGATT 1620
AGGCTATAGG TCTGGGTGGC TCCTGCCTGA GTTCCTGGGG CTCAAGTTAC CCCATATCAA 1680
ACTGGGAGAC CCTGTGTGGT CATTTCTTGG TGCCAGAGTC TGGTTGAGGG GCACAGGCAG 1740
GGAAGCTGGG TCTGGAACAG TCTGTCAGGT TGGACACTGT GATCACCTCC CATTGAAGCA 1800
GGAGGAGGTG 1810
|
