| Tag | Content |
|---|
EnhancerAtlas ID | HS060-12180 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr16:1776820-1779070 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SNAI2 | MA0745.2 | chr16:1778418-1778428 | TGCACCTGTT | - | 6.02 | | Zfx | MA0146.2 | chr16:1777800-1777814 | GCCGCCGCGGCCTC | + | 6.27 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 1777062 | 1777143 | | chr16 | 1777359 | 1777572 |
| Enhancer Sequence | GCTCTGACCT CACACAGACA GGTAGCCTCT CCCGGGGCCA CAGCCGTTGC CGGGGTCAGC 60
ACAAGCCTGG GATGGCTGGT TGGCTCCCTC CTGCAGCAGC CAGTTACATG TGTGCAGCGT 120
GCAGTGTCTA TAACTCGTGT GCTGTGTGCA GTGTCTGTGT GTTGTGTGCT GTGTGCAGCG 180
TCTGTGTGTC ATGTGCTGTG TGCGGCATCT GTGTGAGTCA TGTGCTGTGT GCTGTGTATG 240
AGTGTTGTGT GCTGTGTGTG GCGTCTGAGT TGTGTGCCGT GTGGAGCGTC TGTGTGAGTG 300
TCATGTGCTG TGTGCGGCAC CTGAGTTGTG TGCTGTGTGG AGGGTCTGTG AGTGTCGTGT 360
GCTGTGTGCG GCATCTGAGT TGTGTGCTGT GTGCGGCGTC TGAGTGACGT GTGCTATGTG 420
CGGGTCTGTG TGACTCTGCT GTGTGTAGCG TCTGTGAGTT GTGTGCTGTG TGCAGCGTCT 480
GTGTGAGTGT CGTGTGCTGT GTGCGGCGTC TGTGTGAGTC GTGTGCTGTG TGCAGCGTCT 540
GTGAGCCGTG TGTTATTTAC CATGTGTGTT AGTCACATTT GCTGCATGCA GCGTCTGTGA 600
GTCACATGTG TCACGTGTCA TGTCTGTAAG TCTTGTGTTG TGTGCGGTGT CTGTACATCG 660
TGTGTCAGGT GCAGCGTCTG TAAGTTATGC ATGTTTGGTG CTGTGTCTAA GTCGTGCGTG 720
TGAGGTGCTG TGTCTAAGTC GTGTGTGTGA GGTGCTGTGT CTAAGTCGTG CGTGTGAGGT 780
GCTGTGTCTA AGTCGTGCAT GTGAGGTGCT GTATCTGAGT CACGCGTGTC AGGTGTGATG 840
TCTGTAAGCA CCTCAGGCTC CTTAGGGAAG ACCAGACTGA CTGCTGGCGC TGACGCCTAT 900
GCTGCTCCTC GGGGTGAGAT CCCCGCGCCA GCAGTGCAGC TTCCCTGGGT GCCTGGTAGA 960
GATGCGAGAG CCCAGCGTAG GCCGCCGCGG CCTCCAAGGA TGTGCCAGGC CAGTTACCCC 1020
CCAGATCACA GAGCAGGATG GCCAAAGTGA GATGTTGAGC CACATAATCT GTGGAGTCAT 1080
TTCTAAACAG ACACCAGAAA GCTGGGGAGG ATGGGAGGGC ACCACGCCGA GGACAGGGCA 1140
CAAGCTGGTG GAGCACCTTA CCAGCTGAGT CCCGGCCACG CACTCCCTGG GGCTGTCTCT 1200
CACCTCGTGG CGTCAGCCCT CCCCATTGGT GGGCTGCAGG ACAGAGCTGA GGTTTGAACA 1260
CAGCTGTGGA GGCGGCCATC AGGCCGGGGG CACGCATGCA CCATTGGCGG GACATAGAGT 1320
GGGGTCCCCT GGCTGCGGCT GCCCGTCGGC CTGTCATGCT GCTTCTGTGT CTCTTGGGCA 1380
GATCACGTCT GGGGCCAGAG AGGCCCGTGT TGGTGTCACG GGGGGCCTCC CGTTTAAGGG 1440
AGACATGACT GTCAGCCCAG AAGGCACATA GTCATGATTG GCCTCCCCAG CCCTCGGCGT 1500
GTGTGAGGGA CCTCGCTGCT TGTTCTGCCA GACACGACCC TTTGACGTGT CCAGGAGGTT 1560
ACTCACTTTG AATCCCGCCT CCTCCCGCAA GCTTCTTGTG CACCTGTTGC CTGTGCCTGG 1620
CGTGCCTGGG TTTTGCCTGC ATCTCAGAAG CTTGTGGCTG ACTTTAGCAC AGAGAGCGCC 1680
TGTGGGTTTC CCCACCCCCA TATTTAACTC CCAACAGAGC TGAGTGTTTT CCCATGGCAC 1740
AGGGCACACA CAGCAGCCCC CCAGACGGCC TTCACAGAGC TGAGTGTTCT CCCATGGCAC 1800
AGCACACACA GCAGCCCCCC AGACGGCCTT CACAGAGCTG AGTGTTCTCC CATGGTACAG 1860
GGCACAGCAG CCCCCCAGAC GGCCTTCACA GAGCTGAGTG TTCTCCCCTC GCACAACGCA 1920
CGCAGCAGCC CCCCAGACGG CCTTCACAGA GCTGAGTGTT CTCCCATGGC ACAGCGCACA 1980
CAGCAGCCCC CCAGACGGCT TTAACAGAGC TGAGTGTTCT CCCATGGCAC AGCACACACA 2040
GCAGCCCCCC AGACGGCCTT CACAGAGCTG AGTGTTCTCC CATGGTACAG GGCACAGCAG 2100
CCCCCAAGAC GGCCTTCACA GAGCTGAGTG TTCTCCCATC GCACAACGCA CACAGCAGTC 2160
TCCCAGACGG CCTTGCACTT GCCGGGCTGC TGCTGGTTGC CTCAGGACCC AGAGTCCCAG 2220
CCTTGTCCTG GAACCCCCTC CCTCTGTGGT 2250
|
| |
|
|
|
