| Tag | Content |
|---|
EnhancerAtlas ID | HS098-29957 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr2:46714610-46715750 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr2:46714982-46714999 | TGGTCAAACTAAGGTCA | + | 6.09 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 46714952 | 46715006 | | chr2 | 46714697 | 46715688 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I046487 | chr2 | 46714721 | 46715540 |
| Enhancer Sequence | TTTTTGCCTG GACCTTCCCG TTTCCAGACC AAAAACTTTC TGAGGTCCTG CGTTTGAGGA 60
TTACTTTCAG CTGTAAAAGA AATCCAGCCA CAATGGCTTC ACCAAATAGA GGTTTGTGTT 120
GCTCACATAC CAAGAAGTCC CAGGTAGTCC ATCCACGGCT GGTGAAACTG CTCTCAGAAG 180
TCATAGAGGA CTCAGGTGGT GCCTTCCTCC ACCACCACAG GGCTCTTATC CTCAGCCCAT 240
GGCTTCCCGC CTCAGTGTCA AGTTGGCTGA AGCAGCTCCA AGTACCAGGT CCGTTACTCC 300
AGGTCAGAAA AGGAGCCGCC TTTTAAAAGC ATCCCAGGAA GCCCCACCCA GAGACTTCTG 360
CTTCCGTGCC ATTGGTCAAA CTAAGGTCAT GTGGCTGCAC CTATCTGTAG GGTGTCTGAG 420
GTGGTAAGGT TTTTGCGTGG ACACTGTTGC AGCCTCAAAC AGAATTAGAA TTCTGATAGT 480
ATGAGTGGAG GGGGGAGATA CTGAATTAAG CAAATAACTG GTGTATCATC CCTAATTCCT 540
TAGGCCCAGC TCCCACTCCC TTCCTGAGCT GCTGAGCCAG AAAGCCTTGA TGGGGTTGAA 600
ACCATCAGAT GGAGCACAGC CGTAGCCAAT CTGGGCCGGG CCACTGCTGC ACTCTGCTTT 660
AAGGAAGAGT ACTGCATACC ACAGCAGGGA GGTCATGGTT TTCCCTGGCC ACACGCCTGG 720
AGCCACTCTG CCTTCATCCT CCTGACCTCT GCCTGAAGCC CATGACCTGA CACAATCAGG 780
GCAGCAGACT GGGAAGGGCA CTCCTCTCTG TGCTGGGTGC CCTCAGCAGA GCTGCAAGGG 840
GAGGCAAGTT GGACTCCAGA GCCCCTTCCC TTCCTGATCC CAGATCCCAC AGAGCAGAGC 900
CCAGAGACAG TCAGGGGACT GTGATCATCC TATGGACACC AAGCTGCTAA AGTCTATGTA 960
TAAGAGATTG CACTCATTGC AAAGGACCAC TAAGCTTCAG CCCAAATAAT GAAGCACTAA 1020
TAGTAAAGTT TCAGGCAGGC TTAGGGAGAG AAAGATGGGA AAATCTCTCC TGTTCCCTAA 1080
ATGGAATATT GTAGGCTGCC CTCCTGAGCC CAAGGACAGG ACTACAGTTG GAGAGACTCG 1140
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