| Tag | Content |
|---|
EnhancerAtlas ID | HS165-08655 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr2:234738710-234740050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr2:234738983-234738994 | ATGACCTTGAC | - | 6.32 | | Esrrg | MA0643.1 | chr2:234738983-234738993 | ATGACCTTGA | - | 6.02 | | HEY2 | MA0649.1 | chr2:234739716-234739726 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr2:234739716-234739726 | GACACGTGCC | - | 6.02 | | RREB1 | MA0073.1 | chr2:234739051-234739071 | GGGAGGTGGCTGATTTGGGG | - | 6.48 | | ZNF263 | MA0528.1 | chr2:234738862-234738883 | GGGGCAGGAGGAGAGGGAGAG | + | 7.18 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTCTTCTAGC AGATTCTGTA ACTGGCAGGT CACTTTTGAG TATTAGGACT CAAAATACCC 60
CAAAGTGGTC TTGTCCACTG CCTGCAGGCC CATGTTGGGA TGGGAGCGGG CCTGGCTTCT 120
CCCTCTCCAC AGCCCAGCTC CTCTGTTGCT TTGGGGCAGG AGGAGAGGGA GAGACAGATT 180
TGTTAGTAAA TGTGCCTTCT CATTTGAGTT GCTGCCTCTC AGGCTAACCC CGGCTGGCTG 240
GGGACCTCAG GATCCTCACT CCCTGCATGG CCCATGACCT TGACCGCCCT CTTCTCTCCC 300
TAGTCTCTGC TTACAGACTT GGGGGGTGGG GTCAGGAAGT GGGGAGGTGG CTGATTTGGG 360
GAGGTTCTGC CCCCGCCTAG TAAGCCTTGG GACGCAGCTG GCCTAACATG AAAGAAATGC 420
AATGGTCATT TTCAGCAGGT GCCTTGGACT CCAGCTCTGG GGTCACAGGA CAAGTACTGT 480
CACTATGAGG GCAGCAGTTT CCAGGTGGGG TGGAGCGGGT GGCCCAGATG GCCTGGGTGG 540
CCCAGGTGGG ATGGCCCAGG TGGCCCAGGT GGGATGGCCC TGGTGGCCCA GGTGGGATGG 600
CCCAGGTGGC CCTTACAGGC AGTGAGGGGG ATTGAGATGC ACACTCCCTA GACCTGGGCT 660
TTGCACTCAC CACCCCAGCT TCTGGACTTT GCCACATCCC TCTGCCACAC CATCCCTGGC 720
CACCCTGGGC ACAAGGTGTC ACTGCCCAGA GGCTCCTTTT CCTTGCCAGT CCTCACCACC 780
CTCTGTCTTC AGCCCACACT GTTCTTCCAT GTTTTATCGA CAACTGTCCA GTGGGGTGGG 840
GGGGCTTCAG GGAAGGAACC AGGGTGCACC CAGCAATGGT GACCGAGAGT GAGGAAAGGG 900
CTACCGAGAC AGAAGCATTT TGTCTTCCTG CCCTGCCGTC TCCAGAAGCT GTGGCCAGCA 960
GGCTTGGTCA CAGGCAGATG CTGGTGGACT GGGCCTGGGA GGTGAGGACA CGTGCCCAGT 1020
CTTGCCTGCT CAAGCCCGGC TCCCGCCTCT GATCCCATGG AGGGCTGGGT CCCAGGCAGG 1080
GCTGCTGAGG GCACGAAGGT GCTGGCTGAG GGGGCGGGTG GGGCTGCATC TGCCCCCAAG 1140
GGGCTTTCTA TAAATGTACC TGCAGCCATG TTCAAGCTGG CAGGGGCCCA GGTCCCAGGT 1200
GGCCTCCCAG GAGCCACCAG CCCTGCCTTT CTTTGGCTTG GTGAGGCTTT TCTGGGGCTG 1260
CCCTCTGGCT TCCTGCCAGC CTCACCCCTC TGGGGAACCA CGTGGCCTGG CTGATGGCTC 1320
TGCTGCCGTC CTGTGTCCCT 1340
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