| Tag | Content |
|---|
EnhancerAtlas ID | HS158-09246 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr11:995430-996960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:995740-995761 | TTCCTCCCTCTCCCCTCCCTC | - | 6.24 | | ZNF263 | MA0528.1 | chr11:995735-995756 | CCCTCTTCCTCCCTCTCCCCT | - | 6.79 | | ZNF263 | MA0528.1 | chr11:995744-995765 | TCCCTCTCCCCTCCCTCCACC | - | 7.93 | | ZNF263 | MA0528.1 | chr11:995726-995747 | CTTCCCTCCCCCTCTTCCTCC | - | 8.31 | | ZNF263 | MA0528.1 | chr11:995729-995750 | CCCTCCCCCTCTTCCTCCCTC | - | 8.79 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 995839 | 996019 | | chr11 | 995487 | 996393 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I000996 | chr11 | 995361 | 995470 | | GH11I000995 | chr11 | 995741 | 995890 |
|
Enhancer Sequence | CAGGCGGGCT TTCTGTTTGT CCAGTTAGAG GACCTGTCTC TCCAGGACGC AGGTCCAGTG 60
GTGGCAACCA GTGCTGCTAC CCAGTATCGG CAGGGCTTTG TGGGGTGAGC TCCTGTGGTG 120
GTGCCTGCCC TGGCAGTGTG CTGGTTGGGA GGGTGCTCAT GTCGGAGTCC TGGCACTCCT 180
TGGCGGGGAC CTGCTTATGT GCCCCGGCTG ACCATGTGTC CTGCCCCTCT GGCCGACAGT 240
GCAGGGCCTG CCATGGGGCT GGTATCCAGG CTGAGCCTGA CATCTCAATG AGCAGTCTTC 300
CCTCCCCCTC TTCCTCCCTC TCCCCTCCCT CCACCTAGTG TCCTCTGTGC AGCCCCTGTC 360
CCCCCGTGCC CTCTCTCTGT GTTGTTTGTG GCACGCTGCT GTGCCCGCCA TCTGGAGGCT 420
TGAATTGCCT GTGAGCTCAT CCTGGAGTGA ATGAAATGAA TGAAAGATGT GACTCTTTCT 480
CCCAAGGTGG GCGTCTTCCC TTCACGCCTG AGCACCTTCA TGCTTATGTT TCTCATGTGC 540
TCTGTAGAGC TGGTGACCTG CTTTTGACCC TGTCTCCTCC CGTGGGACGT CACTAGCCAG 600
GCGCCTAGTG CAGCAGGCCT CTGTCACTCC TCTAATCCAT CTCTCCCTCT CCTTTGGACA 660
TCTTGACATA GGTTTCTGGA GGCAGAAACT TGCTTGTGGA GATTTGTCTG TGAGCTGCCG 720
GAGCAGGGGC CTTCCCGTGG GTGCTGGGCC GGCAGCGGCT CCGCCCTGCA GAGAGGAGGA 780
CGCGGCCCCA GTTGGGTGAG GAGGCGAGGG CAGGATGACG TGATCCAGGG GAGGCTGGTG 840
TGCAGGGATT CCTGGAGGCC GGCTTTCAGC AAGGGCACTG TGAAGTCTTC CACGGAAACC 900
TGGGATTGCC TGTTGGAAGC TGGGAAGGCA CCAGGTGCTC TCGCTCCCCT CCAGCTGCTT 960
TGACGTTAAG AGGAACTCGC TGAGGGAGCA TGGAAAGGGG CTGTAGGATT GTCTTCAGTC 1020
TCTCTTTGGT TCTTATTTGA TGTTTCTTTT TAATGTGGGT CCTGAGAAGT GAGGTGTGCC 1080
CATACCCCAG GCCTTTGATC ACACCCAGGT TTGTCCGGCT AGGCTCAGGG TGGACTTTGG 1140
AGGGCCTGGC CTTGACTGTG TGGCTTAGGG ATCAGATGGA AGCTTCTGGA CCCTGGGAGT 1200
GAGAGCAGTG TGCTGCCCTC TGAAAAGGAG GATGAGGGTC CAGTGAGGTT CAGCATTTCT 1260
GTAAGGTGCC TTCTTGGAGG GAGTTCCCCC TTCAGGGCTC ATTCAGTGGA TTTTCTGAGT 1320
GTGGCTTCAC TCCTGATGGT CAGTGGTGCC TGGCGGGTGG GTTCCTTAGG GAGGTGTCTG 1380
TGGCCGAGGC ACGCAGCTCT GTTCTGAGCT GAGAGCTGTG GTGTGTGGGC ACCTCCGTCC 1440
TGACTGAGAG CTGTGGTGTG TGGGCGCCTC CGTCCTGACC GAGAGCTGTG GTGTGTGGGC 1500
CCCTCTGTTC TGACCGAGAG CTATGGTGTG 1530
|
