| Tag | Content |
|---|
EnhancerAtlas ID | HS076-15119 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr12:121417870-121419070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr12:121418141-121418162 | TTTTCTGTCCAAGGTCCTGAT | - | 7.18 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23495 | chr12:121415641-121419989 | Colon_Crypt_1 | | SE_24673 | chr12:121415750-121418798 | Colon_Crypt_2 | | SE_24673 | chr12:121418880-121419524 | Colon_Crypt_2 | | SE_27808 | chr12:121415253-121422996 | Fetal_Intestine | | SE_28751 | chr12:121414723-121423182 | Fetal_Intestine_Large | | SE_32255 | chr12:121415237-121423194 | Gastric | | SE_53251 | chr12:121415308-121420038 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTTCCTGGGC GCTGTGCTGA GGTTTCACAG GAATAATTTC CCTTCATGGT GAGGAGTCCT 60
GGGCAGAAGC TATTGGTGAC TCTGCTTCAC AAATGGGGAA ACTGGGGCTT AGAGCCGGGA 120
AGGAGCTAGA CTAAGTTCAC CAAACTGAGG CCCCAAACCT ACTCTGTTCG GTGCTCTCAA 180
TTGCTATGAC CGGGGACCAG AGGCCTGCAG GGGGTGGCCA GGGAGTCAGA GAGAGACCGA 240
GCCCCAAAGA TGCTCCAAAG GGGCCCATCT CTTTTCTGTC CAAGGTCCTG ATCCCAGCTG 300
GGGTGGGGGA GGGCTGGTGG ATTCCTGCTT TCCCAGAGGC CTCAGGGAGC CTCCCGAGGG 360
CCTGGACAGG GGGCAGGGGA GCAGTCAGGG CCCCCTGACT TGGCAGGAAG AGGAGGGCAA 420
AGGACTCCAG AGCTGCAGGG GAGGGGCAAA GAGTCAGGCA TCCCAGACCC AGGGCGAAGG 480
CAACCTGACG GGGTGGGGCT GGGCCTGACC TGCCCAGGGC CCCAGATGGG ACTGGGGGCT 540
TTGGGGTGAG GGTGGGGGCA GGGGATGCTT TCTTACCTGG CTGAGTGAGC TCTCTCGGTC 600
AGCAGCCCCC TTTGGTGGGA TGGTGGGGTT GGGGAGGCTT GATCCACAGC ATTTGAAGGG 660
GAAGCAGAGG TCAAAGTGCT TCCTAGGGAC CAGCAGAGAC CTGGAAGCTG AGGCAGAGAG 720
TGTAGAGAGA GGCCATTGGG GGAGATGGAC AGAGAAGCTG GGAGAAGCAG AACGGAGGAG 780
CCAGGGGGGC GGGGGCTCAG ACCCAGCTGG GAGAAGGGGC ACGGGAGAGA ATGAGGCGCC 840
CCAAGCTTGC AAGGAGGCTG GAGTGCTTCC CGCCTGCCCC GATTGGGTTT TCTTTAATGC 900
TAACAGCATG CTATTTACTT TCCATTTAAA TTTGAGATGT TGCTATAAAT TATCAACCAG 960
CTCCTTGTTC CTGCAGAGTT TATAACTAAC TACCTGGGTT ACTTATTGTT CAGGTAACAA 1020
AAGGGATCGG AAAACGCCCT GAGTGAAAAA AGTGGGGCCT CCAGCGTCAG GGTCAGGAAA 1080
GGAGCCAGGG AGAGAGGGGC GGGGGACCCC TATTGAAGGC CTGGGCCATT GGGGAGGTTG 1140
AGGCTGGGAA GACGGTACAG AGGCAGAATG TCTAGTAGAA GCTGTTTCCC GGGAGAAGTC 1200
|
