| Tag | Content |
|---|
EnhancerAtlas ID | HS098-29884 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr2:45199390-45200840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr2:45199633-45199654 | TTCAGCCCCAAGGATAGAGGC | + | 6.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 45199818 | 45200000 | | chr2 | 45200000 | 45200797 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I044973 | chr2 | 45200340 | 45200539 |
| Enhancer Sequence | GGCCAACATG GTGAAACCCC GTCTCTACTA AAAATACAAA AATTATCTGG GTGTGGTGGT 60
ACACACCTGT AGTCCCAGCT ACTTGGGAGC CTGAGGCAGG AGAATCACTT GAACCTGGAA 120
GGCAGAGGTT GCAGTGAGCC AAGATGGTGC CACTGCACTG CACTCCAGCC TGGTCTGGGG 180
ACCGAGCTAG ACTCCGTCTC AAAAAAAAAA AAAAAAATGC AGCTCTCTCA TGAGAGTCCA 240
TTCTTCAGCC CCAAGGATAG AGGCTGCAAA AACTGCCCAC GTCATCTGGC CCAGGACACA 300
TCCTGCCTGT GGGGTGGGCT GACCTCATAC CTGCCACATA CTGGGAGCCC AGAGTCCTCC 360
CACTCCAGCC CAGCCCAGTC CAGGGCCACC AGCTCTTAGG TTCTGAAGTA GCCCTTTGAG 420
AGGGTGAGGG TGACATGCCA TGTCTCTCTG TTCCCATCCT CCTGCCAGTC TTCTCTCCAC 480
CCTAGCATTT CAGGCAAAGG AACAGAAAGC CAGTCTGTGC CCCCACCTGA CACTCTCTCC 540
AGGAAGTGTC AGGGAGTGGG CTCTGCTGCC TGGCCCCTCA CGCCAGGCTT CAGGATGAAA 600
GGAAACTCCA GAATGACAAT TTGGGATTAT CTAGTGCCCT GGGCCAGATA GTCTCCTGTG 660
AGGATTAGTG GCATCTTTGA AAAGCAGCGG CCACTCCTTT ACACAATACC TCCTCTTCAG 720
GGGATCTCCT CCCACTCTCC CATACAGGGA GCTCTGAATC TGCAGAGGAC AGCTTATCTT 780
GGAACACCTT TGGGATGGGA AACTGATCAC CTTTCAAGGA AGCCCAGTCC ATCTGCATCT 840
GTGCTAGAAA GTTCTTCCTT CTACCGACTC AGAAGCAGTC TCCCTGCTGT TTCCTCCTTG 900
CATCACGGAG CAAAGCCTGC TGCTTTTTCC AGGAGCAGTG GGGGCACGAA ATGTCCTATT 960
GTTTACGTAC CCAAAGAGTG CTTGCTCTAA GCTCCTTCTC CACGAGAACT CTGCAGCTGC 1020
CGCTGACCAC AGGATGCTCG TTTGGACAAT GAAGCCCCTT TCTAATGGGA GGATACTTTC 1080
AGGATTGTTG CCCCTAGTGA GCTTCCTACT CCTCCCCTTC CGGTTGCCCC CGGTGTGCCC 1140
TCAGGCTCCT GGCAACTCCA CTGCTTCACT CAGCCATCAC TCCAACTAGC TTTCTATATC 1200
TCCATGCCCC TGTGTTCAGT CCTAAGTGGA GCTACTGGAT ATTTGAGCCT CTCACTCAGC 1260
AAGCCTTGGA GCTCCTTCCC TTAAGCCCTA CTAGCACCCT TCCCCCATGC ATGTAGGTCC 1320
CGGGGCCCAG CCACCACTGC AGGCATGGAG GAAGGGGGTG GGCAGTGCAC AGGTATCCAT 1380
GGCAAAGGGC CAGCGGGCTG TATCTGTGGA AACAGAATCT GTAGCCTCCC TCACTGATCC 1440
TCTCTGAATC 1450
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