| Tag | Content |
|---|
EnhancerAtlas ID | HS046-17295 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr19:4083800-4084860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:4084376-4084394 | TCTTCCTCCCTCCCTCCC | - | 6.36 | | HSF1 | MA0486.2 | chr19:4084568-4084581 | TTCTAGAAGCTTC | + | 6.28 | | MYCN | MA0104.4 | chr19:4084542-4084554 | GGCCACGTGGCC | + | 7.22 | | MYCN | MA0104.4 | chr19:4084542-4084554 | GGCCACGTGGCC | - | 7.22 | | Myod1 | MA0499.1 | chr19:4084615-4084628 | TGCAGCTGTCCCC | + | 7.12 | | ZNF263 | MA0528.1 | chr19:4084371-4084392 | CCCCTTCTTCCTCCCTCCCTC | - | 6.14 | | ZNF263 | MA0528.1 | chr19:4084310-4084331 | GGAAGAGGAGCGGAGGGAGGG | + | 6.48 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_00903 | chr19:4083864-4084455 | Adrenal_Gland | | SE_02962 | chr19:4083523-4085082 | Bladder | | SE_12453 | chr19:4083727-4085036 | CD3 | | SE_19502 | chr19:4083630-4085257 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20194 | chr19:4083237-4085170 | CD56 | | SE_22707 | chr19:4083615-4085191 | CD8_primiary | | SE_23073 | chr19:4083139-4085071 | Colon_Crypt_1 | | SE_23728 | chr19:4083583-4084973 | Colon_Crypt_2 | | SE_24683 | chr19:4083592-4085030 | Colon_Crypt_3 | | SE_26575 | chr19:4082693-4085061 | Esophagus | | SE_27700 | chr19:4083659-4085066 | Fetal_Intestine | | SE_28696 | chr19:4083692-4085120 | Fetal_Intestine_Large | | SE_31428 | chr19:4083442-4085057 | Gastric | | SE_42412 | chr19:4083527-4084881 | Lung | | SE_50061 | chr19:4082762-4085231 | Sigmoid_Colon | | SE_53358 | chr19:4083688-4084969 | Spleen | | SE_55380 | chr19:4083851-4084635 | Thymus | | SE_58113 | chr19:4083508-4084948 | VACO_9m | | SE_62529 | chr19:4051126-4090382 | Tonsil | | SE_65287 | chr19:4083611-4084987 | 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 |
| GH19I004082 | chr19 | 4082946 | 4085145 |
|
Enhancer Sequence | CAAAAAATGA GCTGGGCATG GTGGCGCGCG CCTGCAGTCC CAGTTACTCA GGAGGCTGAG 60
GCAGGAGGAT CGCTGGAACC TGGGAGGCGG AGGCTGAAGT GAGCTATGAT GGCGCGCCAC 120
TGCCCTCCAG CCTGGGCAAC AGAGTGAGAC CCTGCCTCAA ACAAAAACGT AAACAAAACA 180
GGAGGCCCTG CTCTCCTGAG GGGCTGGTGG TGAGTCACTG GTAGATGGGA GAGAGCTGGG 240
GTCAGGGTCC CAGCTGGGGG GGTGGGTCCT CACCTGTGCT ACCCTCCAGG GGGCCTCTCT 300
CCAGGCCTCT GTCCCTCCCC TGGGAAGCCT GGCAGAAACC TGAGACTGGG CCTCCAGTTC 360
CAGGTCGCCA CTGGGCCCAG GCCTCTCCTG TCCGCCTGCC AGGGACTGCG GAACAGGTAA 420
CTCCTGCGCC ACCCTAAACC CACCTGGCCT GTTGCTCCAG GTGCGGCCTG GAGGCCCCGG 480
GGCCTGCACA CCTGGTCAGC TCAGAGGCCA GGAAGAGGAG CGGAGGGAGG GGTGGGGCCG 540
CCGGCCGCTG CTGGTTTCGT TTTGAGCCGG GCCCCTTCTT CCTCCCTCCC TCCCACTCCT 600
CGCCAGACCC CTGCATTCTG GGAAAGGCTG TGACAACTTC CTCTGAACTC TCCTTAACCT 660
GCCCTGGAGC CCAGGGCCTC CAGGAGGCTG AGTTCCGCCT GCGGGACCTG AGGCTTCCTG 720
CAGGTCACAC ACCTCCACCC CTGGCCACGT GGCCCTAGAC CGCCCACCTT CTAGAAGCTT 780
CTTTATGTGC TGCCCCATCA TGTCCCCACC CCGGGTGCAG CTGTCCCCTG CCTGCACCCC 840
CTCCACCCTG TGTCCCAGAC TCTGCACACA GGAAACCGCC CTGGCCCCAG GGAGGGCTGC 900
CTGAGACCCC CGCCTCCAAC CTGCACTGGG GACATCTGGG CTGGATGGTC CTCGGGAGGT 960
GGGGCTGCCT TGGGCACTGC AGGGTGCTGG GTGACATCTC TGGCCTCCAT CCATTCCATG 1020
GCAGGGGCAC CCCCTGTCTC GACAACCACA GACGTCTGGG 1060
|
