| Tag | Content |
|---|
EnhancerAtlas ID | HS095-14394 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:4083840-4084800 |
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 | CAGTTACTCA GGAGGCTGAG GCAGGAGGAT CGCTGGAACC TGGGAGGCGG AGGCTGAAGT 60
GAGCTATGAT GGCGCGCCAC TGCCCTCCAG CCTGGGCAAC AGAGTGAGAC CCTGCCTCAA 120
ACAAAAACGT AAACAAAACA GGAGGCCCTG CTCTCCTGAG GGGCTGGTGG TGAGTCACTG 180
GTAGATGGGA GAGAGCTGGG GTCAGGGTCC CAGCTGGGGG GGTGGGTCCT CACCTGTGCT 240
ACCCTCCAGG GGGCCTCTCT CCAGGCCTCT GTCCCTCCCC TGGGAAGCCT GGCAGAAACC 300
TGAGACTGGG CCTCCAGTTC CAGGTCGCCA CTGGGCCCAG GCCTCTCCTG TCCGCCTGCC 360
AGGGACTGCG GAACAGGTAA CTCCTGCGCC ACCCTAAACC CACCTGGCCT GTTGCTCCAG 420
GTGCGGCCTG GAGGCCCCGG GGCCTGCACA CCTGGTCAGC TCAGAGGCCA GGAAGAGGAG 480
CGGAGGGAGG GGTGGGGCCG CCGGCCGCTG CTGGTTTCGT TTTGAGCCGG GCCCCTTCTT 540
CCTCCCTCCC TCCCACTCCT CGCCAGACCC CTGCATTCTG GGAAAGGCTG TGACAACTTC 600
CTCTGAACTC TCCTTAACCT GCCCTGGAGC CCAGGGCCTC CAGGAGGCTG AGTTCCGCCT 660
GCGGGACCTG AGGCTTCCTG CAGGTCACAC ACCTCCACCC CTGGCCACGT GGCCCTAGAC 720
CGCCCACCTT CTAGAAGCTT CTTTATGTGC TGCCCCATCA TGTCCCCACC CCGGGTGCAG 780
CTGTCCCCTG CCTGCACCCC CTCCACCCTG TGTCCCAGAC TCTGCACACA GGAAACCGCC 840
CTGGCCCCAG GGAGGGCTGC CTGAGACCCC CGCCTCCAAC CTGCACTGGG GACATCTGGG 900
CTGGATGGTC CTCGGGAGGT GGGGCTGCCT TGGGCACTGC AGGGTGCTGG GTGACATCTC 960
|
