| Tag | Content |
|---|
EnhancerAtlas ID | HS095-17769 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:231692580-231694740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr2:231693149-231693164 | AGCTAGGGCGTGGCC | - | 6.01 | | RREB1 | MA0073.1 | chr2:231694109-231694129 | CCCCAGACCACCACCAGCCA | + | 6.74 |
|
| | 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 |
| GH02I230828 | chr2 | 231693116 | 231693315 |
|
Enhancer Sequence | TGCGCCCTCT TCCAAATGCC TGGCTTCCTC CAGAACCTCC AGAGCACATT GTTGGGGCCT 60
GAGGAGCAGT GCCAAGGGTC CCGGAATCCC ATCTGCTCTG ATCAACAGTC ACAGGACCGC 120
CGACGAGGAA AGAGGATTTG CCACCGTCCC CTGACAGGTT AGAACCAGAA CGTTCCGCCC 180
TGCTGGGCCC AGGGCCAGGC TCGGAGCAGG CTTCTCAAAC TGCAGGGTCC ACGCCACCCA 240
TCGGGGGTCT GGCGGTCTAG GGTGGGGCCC GAGACTCCAA ACTAGGCTGC CGTGAGGACC 300
ACACCGGGAG GCGCCGTGGG GGGCGGGAGA CCTCAGCCGC GGGGCGGAGA AGGGCCAGGC 360
GCGCGCTCCT GGAGGTACGG GGCGCGCAGC CCCGAGGTGT GCCCGGGCCG AGGTGGGCGT 420
CTCCCGGGCG CGCCCGGGCG TATGGCGGCG TCGCTGGGAT GCCAGATCCC AGGGAGCTCA 480
CCGAGGCCAC GCCGATGGCC ACCCGGGTGG AGCCTGGGCT GTGGGCTTCG CCTGCGTCCC 540
CGCGGCCTGT CCACGCGTCC GGCACCCGGA GCTAGGGCGT GGCCAGGTCG GAAGCCGGCT 600
TAGCGCGCCT TTCACCCCTG GCCCCACCCA GGGCTCAGCC CAGCGCCGCG GCGGGCCCGG 660
GCTCCCAGGT CTGCGGCTTT CACTGGGCCG CGTCCCTGCA GAGGGCCCCG GCGACTGGGG 720
AGGAGGCCGC CCTTTCCTTC CGGCCCGCGA CCGCCCCGGG CTGTCCCTAC CCAAGGGAGA 780
CTCCCAGCGG CCCGGAGCCT CAGACTCTCC GGGAGCCAGG CGGCGGCGCC CCAGGGCTGG 840
GGCCTTGGAG CCTGGGAAAG CAACCGGGGG TCTCTGGGGA GTCCTGAGCG CAGGCGCCCG 900
CCCACGGCCA AGACCGTGGC CCAGCCCTCC TCAGACCTCC CAAGGGGGCC TGCCTGTCCC 960
TGCGGCCTGA GAGCCTGTCC CTGCTGCCCC GACGTCCAGT CCCTACTGCC CCGAGGTCCT 1020
GTCCCTGCGG CCCTGCCCTT AGAGCCTCTC CCTGCTGCCC CAGAGCCTGT CCCTGCTGTG 1080
TCGAAGGCCT GTGCAGGACT CGAGGCCGTC TCCCACTCAG AGGGCCTGTC CTTGCTGCCC 1140
CAAGGGACTG TCCCTGACGC AGGGCCTAGG CCTGGAAAGT GGACACTCAA GAGTCCCCAG 1200
GTGATGTTTG GGGTCCGTCT GCCAGAAAGC TGTTCTGCTC CGATGGCGGC GGCAGCCTCT 1260
GCCTCCCCCA CTGAGTGCAG GACTCAGCTC TTCCTGGCTT GGGGTGCAGT GCAGAAGGGG 1320
ACCCTCCTTG AGCCCTGGCA AGCACGGGAG GCGCTTCTGC AAGAGGCAGC TGCTGGCTGA 1380
GCCTGGTGCC CAGGGAGGTG GTGACGAGGA CGCACTCCTT CCAGTTCACT GGGCGACTCT 1440
AAGGGACACC AATACAGGGA TTGGTGGGCC GGCCCCCCGA GAGAGTCAAG GGAAGAAGCA 1500
ATACACATGG TGTCGCCCTG CTCAGTCCAC CCCAGACCAC CACCAGCCAG GCGTGGAGAC 1560
AGGACCAGAA GGACAACTGC TGGGCTCTGG GGGTGCTGAG CAGGGGTGAA AGCGTCCTAG 1620
AGGCTTGGTG CCGACCTGGA CACGGCCCGG CCCAGGCGTG GACTCCCCAC TTGGGAGCGT 1680
TTGTGAAGTG AGGAGAACCC CATGCCACTG CCACATGGCT TCTGTCACCT GCATCCAGTC 1740
ACAGTTCCTG AGGAAAGGGT CCCCGAGATC CCCGTTGGCC ACACTAGGTG CGAGGGAGGA 1800
AGCCTGGGCC AGTGGCTGTC CCTATGGACA CCGCGGGTGG TTTCTCGTTG ACATACATGG 1860
GAACGTCGCT GAGGCCAGGA AGACGGCAAA TCCTTTATTC CTTGTATAAG AGGTGGGCCT 1920
TTGACCCAGA CCTGCAGTTG TGAAGGACAA AGTGTTAAAA ACTGTCTCAG TGAAAGATCC 1980
TGTCAGTTTA AATATTACTA CATTTTGAAA ATGTGAGAGA CGAAATGTCA AGTTCATGCA 2040
GGCATTGAAG CCAAGTGCAA TGGCAGGACA TGTGCTTCCC CTCTCCCCAG CCTGCTTTCC 2100
TCAGCTCTGT GCAGGCCGGA GAGAGTAAGA GCTACCTCCT AGGTCTTCTG TGAGCACTAA 2160
|
