| Tag | Content |
|---|
EnhancerAtlas ID | HS105-20832 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:121340250-121341640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr12:121341532-121341545 | GCGCCCCCCCCCC | + | 6.1 | | ZNF740 | MA0753.2 | chr12:121341534-121341547 | GCCCCCCCCCCAC | + | 6.29 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27043 | chr12:121340195-121348599 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TAATTATAAT TAATGTAGTA AGATCTGTGG CACTTCACAG TTTGCCAAGT GCTTTCTAAA 60
TGTACTCACT TAATCCTTAC AGGCTGTGGA AAAGGTAATT CCCTCTATTT TATAGGTAAG 120
GAAAAAGGAC CGAAGAACTC ACTACCATGT CGTATCAACA AAGCAAGTTG GTGGCAAACC 180
GGACCTCCGA AATAGGTCTT CCAACTCCAC ACGGCATGCT CGTCCCATTC TATTATGCTC 240
TTTTCTAAGA AGGGAATGTC TACAGTTCTG TCCCAAACCA CATTTGCTTC AAGAGTAAAC 300
CATCTTCAAA CCATTTCTCT AAATTGCAAT CAGGTCCCCC ACTCCTACGA TCATGCCATT 360
TCTTGCTTCC TCACTCTCCA GCTATGACTT CCTTCTCACT ACCCGATTTC CACTCTTCAT 420
GGATACTGCC ATCATTCCTT CAACCCGTCC TGCAAATATC CCACCTCTAC ATGCTAAAGG 480
GAGACCCCTC ATGTTCCTTC CCCCAAACCC TGGCACTCCC TTCTCCGGAT ATGTAGGTTG 540
TCACCCCATA AACTACACAG TAGCTTCTCG CTTCTCGGCC CTTAACGAGC TACTTACTAA 600
CTTTAAAAGC CCCACAGAAA TGAACTTAAC TTGCAGGTCC TCCACCTCCA CACTTGGCCC 660
TGGGCGCCAT TCCTCTGAAA ATAATAGTAC CAACCCTTAC AAAGACTCTG CCCATGCCCC 720
ACTGTCACCA ACGAATTCCT TTTCCAGAAG GAAAAGGAAA CAGGTTCTTC AGGCTCCTCT 780
TCCAACCTCT TCACCAGTGA CTCCCCTCCA AGGTTCGTGG ACTCTACCCC CGCAGTTTTC 840
CTCCCCTCAC TCCCGGGCCT CTGCCCACCT CACCAACTCT CCCTGCGCTC CCTGTCCCAG 900
AGCCAAGCGG CGGCCGCTCC ACTCTCCCAA CTTAGAAGTT CTGCCTCTAT CACCTGTTCT 960
CACTAGAGCT TCCTCTCAGC CCAGCGGCCC ACCTTTGCCC TGGCCTGCCT CTCTCCACCC 1020
CTTCGAGTCC TCCTGCCCAG GAAACACCCC CACGAGTCAG TTCCGGGGTG CCTGTCGGAT 1080
TCAACTTCCC ATCCGTGGGA TTCCCACCCC CGGGGTCATG CTCCCCTTCT CCATCACCTG 1140
CTCCGCCCAT AGCCAGATGA CATCCGCCGC TGCCTCCTCC TCCATTCCCC TTCTCGGACG 1200
CCAGGTCCCC GGCCACTCAC CGCCCTCCGT GCGCGCCAGC CGCCCCCTCC GGTGGGGAAG 1260
AGGGGGGCGT GCACCCCAAC CCGCGCCCCC CCCCCACGAC ACGCACCTGT TCTTCCTCCT 1320
CTTCCCCTCG GCGGGCCGCG CCGGCGCCCC GACCCCCACC CTTGCCGCCT CCCGGCCTCC 1380
CGGAGCCCCG 1390
|
