| Tag | Content |
|---|
EnhancerAtlas ID | HS034-14399 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:4083720-4084870 |
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 | GATTGCTTGG GGCCAGGAGT TCCAGGAGTT TCAGGCCAGC CTGGGCAATA CGGTGAGACC 60
CCATCTCTAC GAGAAAGTTT CAAAAAATGA GCTGGGCATG GTGGCGCGCG CCTGCAGTCC 120
CAGTTACTCA GGAGGCTGAG GCAGGAGGAT CGCTGGAACC TGGGAGGCGG AGGCTGAAGT 180
GAGCTATGAT GGCGCGCCAC TGCCCTCCAG CCTGGGCAAC AGAGTGAGAC CCTGCCTCAA 240
ACAAAAACGT AAACAAAACA GGAGGCCCTG CTCTCCTGAG GGGCTGGTGG TGAGTCACTG 300
GTAGATGGGA GAGAGCTGGG GTCAGGGTCC CAGCTGGGGG GGTGGGTCCT CACCTGTGCT 360
ACCCTCCAGG GGGCCTCTCT CCAGGCCTCT GTCCCTCCCC TGGGAAGCCT GGCAGAAACC 420
TGAGACTGGG CCTCCAGTTC CAGGTCGCCA CTGGGCCCAG GCCTCTCCTG TCCGCCTGCC 480
AGGGACTGCG GAACAGGTAA CTCCTGCGCC ACCCTAAACC CACCTGGCCT GTTGCTCCAG 540
GTGCGGCCTG GAGGCCCCGG GGCCTGCACA CCTGGTCAGC TCAGAGGCCA GGAAGAGGAG 600
CGGAGGGAGG GGTGGGGCCG CCGGCCGCTG CTGGTTTCGT TTTGAGCCGG GCCCCTTCTT 660
CCTCCCTCCC TCCCACTCCT CGCCAGACCC CTGCATTCTG GGAAAGGCTG TGACAACTTC 720
CTCTGAACTC TCCTTAACCT GCCCTGGAGC CCAGGGCCTC CAGGAGGCTG AGTTCCGCCT 780
GCGGGACCTG AGGCTTCCTG CAGGTCACAC ACCTCCACCC CTGGCCACGT GGCCCTAGAC 840
CGCCCACCTT CTAGAAGCTT CTTTATGTGC TGCCCCATCA TGTCCCCACC CCGGGTGCAG 900
CTGTCCCCTG CCTGCACCCC CTCCACCCTG TGTCCCAGAC TCTGCACACA GGAAACCGCC 960
CTGGCCCCAG GGAGGGCTGC CTGAGACCCC CGCCTCCAAC CTGCACTGGG GACATCTGGG 1020
CTGGATGGTC CTCGGGAGGT GGGGCTGCCT TGGGCACTGC AGGGTGCTGG GTGACATCTC 1080
TGGCCTCCAT CCATTCCATG GCAGGGGCAC CCCCTGTCTC GACAACCACA GACGTCTGGG 1140
AGTTTCCAAG 1150
|
