| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08663 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr22:47044940-47046000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr22:47045853-47045866 | TTCTAGAAAGTTC | + | 6.41 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_01530 | chr22:47044879-47047235 | Adrenal_Gland | | SE_24734 | chr22:47044954-47045554 | Colon_Crypt_3 | | SE_26636 | chr22:47044960-47046720 | Esophagus | | SE_28507 | chr22:47044906-47046222 | Fetal_Intestine | | SE_31503 | chr22:47044889-47046803 | Gastric | | SE_40615 | chr22:47044753-47050841 | Left_Ventricle | | SE_42318 | chr22:47044799-47050085 | Lung | | SE_49769 | chr22:47044850-47047031 | Right_Ventricle | | SE_50122 | chr22:47044824-47049861 | Sigmoid_Colon | | SE_52376 | chr22:47044785-47047043 | Small_Intestine | | SE_65411 | chr22:47044553-47061547 | Pancreatic_islets |
|
| | 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 |
| GH22I046648 | chr22 | 47044721 | 47047167 |
|
Enhancer Sequence | CTTTAAGGCC TTACTGGCCA CCTTCCAGAG CTCCAGATGC ACCACCTTGC TCCCATTCTG 60
TCTGGTGTTT GGTCCCAGAT GCAGTTTTAT CTGTGCCACC TTTGCTTCCT AGTGCTTTGG 120
GGCCTAGAGT CACCAGCTGG AACTGGAGTT GGGGAGTGTC CCTGATTGCC CCTAGCCCAC 180
ACTCAGCAGG GAGCAGGTGC TTGGCAGAGA GCCTGTTGCT GTGGGAAGGG ACTGGGGGCC 240
TGGAGGGCTT GGCTGCTGGG TGCCAAGCGC TTGGTTGGAA AGGGAGGTTG TGGGGGCGAG 300
GGATGGCACG TGCTGTCGAG CACACGACTC TCCTGGCTCC GTGCTGGGCC GGAGCCCCAG 360
AGTCCAGCCC ACAGGCTGTC AGATGCCGCG TGCCTCTCAC AGGGAGAGGC AGGCGTCGGT 420
TTCTGAAAAC CAGCTGCTCT GGGTGAAAAC CCTGGCTGGG ATCCTAGTTC TTCTTATTTG 480
ACGTGGTAAA AATGTCAGTA CATTATCTGT CCACCTTAGA TCCTGCATTG GTGTCCTGAA 540
ATGTACCTAA AACGGTGGTT GGCCAGCTAT GTGCTCAGCA GCCTTCAACA TTAGGATGTG 600
ACGCACTTGG AAGCTTGCTC CTTCCTGGTT ATCAGCCAAG ACAGTGTTGA CAGTTGATCG 660
TTCAGTAAAC ATTATCTCTG CACATAGCGG TAAATGACAC CGCAATAAAT AAATGTTAGG 720
GAGAAAATGC AGGCAAAACT TCACAATAAA AGCGAGGCAT TTCTTGGAAT TCTCTGTTTT 780
CCCTGAGCAG GGAGGGCCAC GGGAGGAAGG GGTTAAAAGG GCTGCCTCTG TGCTGGTGGC 840
TGTAGATGAA GCCGTACTCT GGGCTCTGCA GTGTAACTTG CAGCCTGGTG ATTCGATGGA 900
GGGAGTGCCT GTCTTCTAGA AAGTTCCTGT GGTGATGGCA GGAGGGCTGA ATTGGGCTGG 960
GAGAGTTCAG GTGAGAGTCC GGGGGAGGTG GCCAGGTGGG GCCTCTGGGT GTGCGGGCCT 1020
CCGGGGATGC GGGACTCCGC CAGGCCAGGA GCAGCTTTTT 1060
|
