| Tag | Content |
|---|
EnhancerAtlas ID | HS073-07133 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:4083770-4084900 |
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 | CGGTGAGACC CCATCTCTAC GAGAAAGTTT CAAAAAATGA GCTGGGCATG GTGGCGCGCG 60
CCTGCAGTCC CAGTTACTCA GGAGGCTGAG GCAGGAGGAT CGCTGGAACC TGGGAGGCGG 120
AGGCTGAAGT GAGCTATGAT GGCGCGCCAC TGCCCTCCAG CCTGGGCAAC AGAGTGAGAC 180
CCTGCCTCAA ACAAAAACGT AAACAAAACA GGAGGCCCTG CTCTCCTGAG GGGCTGGTGG 240
TGAGTCACTG GTAGATGGGA GAGAGCTGGG GTCAGGGTCC CAGCTGGGGG GGTGGGTCCT 300
CACCTGTGCT ACCCTCCAGG GGGCCTCTCT CCAGGCCTCT GTCCCTCCCC TGGGAAGCCT 360
GGCAGAAACC TGAGACTGGG CCTCCAGTTC CAGGTCGCCA CTGGGCCCAG GCCTCTCCTG 420
TCCGCCTGCC AGGGACTGCG GAACAGGTAA CTCCTGCGCC ACCCTAAACC CACCTGGCCT 480
GTTGCTCCAG GTGCGGCCTG GAGGCCCCGG GGCCTGCACA CCTGGTCAGC TCAGAGGCCA 540
GGAAGAGGAG CGGAGGGAGG GGTGGGGCCG CCGGCCGCTG CTGGTTTCGT TTTGAGCCGG 600
GCCCCTTCTT CCTCCCTCCC TCCCACTCCT CGCCAGACCC CTGCATTCTG GGAAAGGCTG 660
TGACAACTTC CTCTGAACTC TCCTTAACCT GCCCTGGAGC CCAGGGCCTC CAGGAGGCTG 720
AGTTCCGCCT GCGGGACCTG AGGCTTCCTG CAGGTCACAC ACCTCCACCC CTGGCCACGT 780
GGCCCTAGAC CGCCCACCTT CTAGAAGCTT CTTTATGTGC TGCCCCATCA TGTCCCCACC 840
CCGGGTGCAG CTGTCCCCTG CCTGCACCCC CTCCACCCTG TGTCCCAGAC TCTGCACACA 900
GGAAACCGCC CTGGCCCCAG GGAGGGCTGC CTGAGACCCC CGCCTCCAAC CTGCACTGGG 960
GACATCTGGG CTGGATGGTC CTCGGGAGGT GGGGCTGCCT TGGGCACTGC AGGGTGCTGG 1020
GTGACATCTC TGGCCTCCAT CCATTCCATG GCAGGGGCAC CCCCTGTCTC GACAACCACA 1080
GACGTCTGGG AGTTTCCAAG CCTCCCCTGG GTGGGGGGAC AGAATTGTTC 1130
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