| Tag | Content |
|---|
EnhancerAtlas ID | HS092-13619 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:121340240-121341640 |
Target genes | | Number: 25 | Name | Ensembl ID |
|
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 | TTCTCTAGGA TAATTATAAT TAATGTAGTA AGATCTGTGG CACTTCACAG TTTGCCAAGT 60
GCTTTCTAAA TGTACTCACT TAATCCTTAC AGGCTGTGGA AAAGGTAATT CCCTCTATTT 120
TATAGGTAAG GAAAAAGGAC CGAAGAACTC ACTACCATGT CGTATCAACA AAGCAAGTTG 180
GTGGCAAACC GGACCTCCGA AATAGGTCTT CCAACTCCAC ACGGCATGCT CGTCCCATTC 240
TATTATGCTC TTTTCTAAGA AGGGAATGTC TACAGTTCTG TCCCAAACCA CATTTGCTTC 300
AAGAGTAAAC CATCTTCAAA CCATTTCTCT AAATTGCAAT CAGGTCCCCC ACTCCTACGA 360
TCATGCCATT TCTTGCTTCC TCACTCTCCA GCTATGACTT CCTTCTCACT ACCCGATTTC 420
CACTCTTCAT GGATACTGCC ATCATTCCTT CAACCCGTCC TGCAAATATC CCACCTCTAC 480
ATGCTAAAGG GAGACCCCTC ATGTTCCTTC CCCCAAACCC TGGCACTCCC TTCTCCGGAT 540
ATGTAGGTTG TCACCCCATA AACTACACAG TAGCTTCTCG CTTCTCGGCC CTTAACGAGC 600
TACTTACTAA CTTTAAAAGC CCCACAGAAA TGAACTTAAC TTGCAGGTCC TCCACCTCCA 660
CACTTGGCCC TGGGCGCCAT TCCTCTGAAA ATAATAGTAC CAACCCTTAC AAAGACTCTG 720
CCCATGCCCC ACTGTCACCA ACGAATTCCT TTTCCAGAAG GAAAAGGAAA CAGGTTCTTC 780
AGGCTCCTCT TCCAACCTCT TCACCAGTGA CTCCCCTCCA AGGTTCGTGG ACTCTACCCC 840
CGCAGTTTTC CTCCCCTCAC TCCCGGGCCT CTGCCCACCT CACCAACTCT CCCTGCGCTC 900
CCTGTCCCAG AGCCAAGCGG CGGCCGCTCC ACTCTCCCAA CTTAGAAGTT CTGCCTCTAT 960
CACCTGTTCT CACTAGAGCT TCCTCTCAGC CCAGCGGCCC ACCTTTGCCC TGGCCTGCCT 1020
CTCTCCACCC CTTCGAGTCC TCCTGCCCAG GAAACACCCC CACGAGTCAG TTCCGGGGTG 1080
CCTGTCGGAT TCAACTTCCC ATCCGTGGGA TTCCCACCCC CGGGGTCATG CTCCCCTTCT 1140
CCATCACCTG CTCCGCCCAT AGCCAGATGA CATCCGCCGC TGCCTCCTCC TCCATTCCCC 1200
TTCTCGGACG CCAGGTCCCC GGCCACTCAC CGCCCTCCGT GCGCGCCAGC CGCCCCCTCC 1260
GGTGGGGAAG AGGGGGGCGT GCACCCCAAC CCGCGCCCCC CCCCCACGAC ACGCACCTGT 1320
TCTTCCTCCT CTTCCCCTCG GCGGGCCGCG CCGGCGCCCC GACCCCCACC CTTGCCGCCT 1380
CCCGGCCTCC CGGAGCCCCG 1400
|
