| Tag | Content |
|---|
EnhancerAtlas ID | HS064-03783 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr12:133068630-133069950 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr12:133069231-133069241 | GGTCACGTGC | + | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_06575 | chr12:133067312-133070596 | Brain_Hippocampus_Middle | | SE_24669 | chr12:133069602-133069890 | Colon_Crypt_2 | | SE_32237 | chr12:133066699-133068967 | Gastric | | SE_32237 | chr12:133069017-133072622 | Gastric | | SE_41687 | chr12:133067304-133073689 | LNCaP | | SE_47660 | chr12:133069127-133069484 | Pancreas | | SE_47660 | chr12:133069607-133072443 | Pancreas | | SE_65399 | chr12:133067333-133086073 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGCTGTCTT CTGCCCTCTC AGTGGTGATA ATGACACAGA CTGTACGTGT ACTGAGCAAT 60
ACTGCAAGCC AGGCCCTGCG CTCGGCTCCT GCACTGCAGC TGAGACCACG AGGATGCCCA 120
CTTTCCAGAG CTGTCGCCAC CCACCTGCAC CTCCTGGGTC CCTAACCGCG GCTTCCTCAC 180
TGCTCCGAGC GGGTCAGCCC TTGTACCCTG CCGTTCTCTG TCTGCTTTAT GTTTGGTGCC 240
ATTGTGTCTT TGCAAAAACG TCACCTCAGA CTCCTCTGAA GTGGTGCCCC CCACCCCCGT 300
CGACGTTGCC CACCTTCTTT TTGTCATCCC CACTCTGCAA AGCTGTTTTA GAATGTCTTT 360
GCTCTCCATT TTCGTCTCCC ACAAGAACTT GTAAGCTGAA AGAGAGCAGA CACTGTGCTG 420
TCCTGTGTGT CTCCTATGGG GTCTGGTGCC GGGAAGAGCT CGATGTGTAG AAAGTGCCCC 480
AGATGCGTGT GTCAGGAATC TGAGTGAGGA GATGAACTGT ACTCAGGAGA TCCAGGGCCA 540
ATCCCAGGCC CACGTGTTTT GCCCGCAGCG GCTCTGACTG GCTGTCCACC TGCTCTGGCA 600
GGGTCACGTG CCCCCAGCCT GCAGGCAGTG GGTTCAGTGG GTTTTGGTGA CTTCGGCTTA 660
GACCAGCTGG CCCCTCAGGT CATAGTGAGA CAAGTCTGCT GCTGCGTGGC GTTAACACAG 720
CCACAGCACC CCAGGGTGGT TTCATGTCCC TTCCTCTGCC CTTCGGAGCC TGCCTGGGAA 780
AGTACGGGGC TTCTGCACAA GTCATAACCT CGTGATCATC CCATACGTGT CTCTTGGTTG 840
TCTACATTTT TTGCCAAAGT ATGGTGGTTT TTCCCCAAAG TTCAGATAAT TCATAATTAT 900
ATCAATAGTA GTGACTGGTT CAGTAAGCAT TCTCTCCATC AGGCAGTGTT CTGAGCTGCC 960
TTTCACAGAC ATCAACTCAT TTACTCCTCA AATGACCCAC GAGGAGGGCT GGATGCCCCC 1020
ATTCCACAGA TGGGGACCTT GAGGCTCCCC ATTGAGGCAG AGCAAGAGCA AGGAGCACTG 1080
GGTGCCACGC CTGTCCGGCC TTAGAGTGAG CGGGCGCTGC CCTGCGAGGC CACCCACACG 1140
GGACACCGAG GGAGATGTGG CCACCAGGAC CCAGCCCAGA GGCACAGCCT GCCCTTGGCT 1200
CTGCCGCCTT TGCTCACAGT CCCTCTGCCC CCACCCGCGT CTTGAGGGCT CTTCCTACTC 1260
TGGGATGCTG GAGGATGGGA CGCTCAGGAG TTGGAGGAAG CCCTTGTAAC CCCAGAGGCT 1320
|
