| Tag | Content |
|---|
EnhancerAtlas ID | HS098-37368 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr22:46298820-46300240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr22:46299881-46299902 | TGCTCTGTCCACGGTTGTGAA | - | 6.57 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I045903 | chr22 | 46298882 | 46299909 |
| Enhancer Sequence | GCGGTAGAAA ACTGGAAATC CCAGAAAAGG AGAAGGAAGA TGCCACCCCT CATCTACTTA 60
ATGCCGAAGG GGGTGTCTGG CTGCAGAAGA CCCTGGCCCT GGGCCGGGCT GGGGGACTCC 120
GTCCTCACTG GGGACAGCTG AGCACAGGGC CAGCTGGGAG GAGGGTCAGT GGCACTCAGG 180
AGAGCCTCCC AAAATGTGTG AATCACAGCG TCTTGGAAGG ATGTTCTCCT GGCTCAGGAA 240
GCGCCCCCTC GATGCCACTG CAGCCTGGCC CAGAAGCCAG GGGGACTCGG TTCCTGCTGC 300
TGAGGGGGTC CCAGGTTGGT GGCCCAGCCT TTGGAAGGCA TGGAGGGGCA GGGACGCCCA 360
CAGCCTGTGC TAGGACAGGC ACCTGAGTCC CCTCCTGGTG CCCCATCCCA GCATCTCTGA 420
GCTACCCCAG GGTACCCTGC GTCCTCCCAG AGGTGGTGGC GGGGCTGGGG CTGGGTGGTG 480
ACATCATGGG TTGAGCTGTG CCAGTTCTTT CCCGACCTCG GAAACCCCAA CATCCCGCTC 540
CAGGAACTGG CCTGCGGCGT TGGCTTTGGC TGGGCGCCCC AGGAGTGTGG CAGGGAGGCC 600
CGGGGCCCCC ATCCCCCCAG CAGTCAGCCC TGAGGCCCCC CCCTTCCCTT CGGGGGCTCC 660
CAGGGAGCCT GGGCCAAGTG TGAGAACCAG CAGGGTCAGC TCCTCAGGTC CTGCCCCCGC 720
CCCTGCCCCT CCTCTACTGC AAGAAAAATA AACAGCTGTC CCGTCTCTCT GAGACTGGAA 780
ACACCACCGC AGCCGCAGCC TCGGCCGAGC TATGGGGCTG ACTCACTGCC CGCCCTGGGC 840
GGGGGCAGCG AGAAGGGGCC GGGGCTGCCC TGAGGAGCCC TGTGGTGACC CTTCTTTCCA 900
CTGTGCCAGG GGGACGGGAG GACACGTCCA TCTCAGGACT CCTGAGCTCG GCCACGTCAC 960
CCTGCTCTCC CTCTGGCCAC TCTGTGACCT TTGTCAGCCA GGCCTTGACC TCTCCTGGCC 1020
CCAGGGTCCT CATCGGCCCA AACGCAGGCT GGAGCATCTC TTGCTCTGTC CACGGTTGTG 1080
AACAGGGAGG AGCATGGTGG CTGGGTTCAG GGGTCCACCC TGGGGCCTCA TGTAGTAGAG 1140
CAGGAAAATA AATGTGTCGG AGTGACTTTC ATCAAGGGTG GAAATGGAAA CCTGTGTTCC 1200
TGGGCGCCTC GATCATTCGG GAATCTGATG ATCCTGAAGT CACCATCGGT CTCCCACGCC 1260
TCCTGCGCTC GTCCTTCAAG CCTTCTTTCT TTTCCACGGA TACCTTCCAG TGTTCCCAGG 1320
CCAGCTCCCT CCTGTGGGTG GAGGGCGTGG GCAGGAGGGC AGTCCCTTTT CTCCGAGACC 1380
CTTGGTTGAA GCTCCAGGCA GCTTCTCAGA GCCTTACAGC 1420
|
| |
|
|
|
