| Tag | Content |
|---|
EnhancerAtlas ID | HS029-07432 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr19:4083590-4085030 |
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 | ATCTTCCCCA AGGTCACAGG CCCAAGGACA GCAGAAATAT CGTCAGGCCT GTGGTCCTGA 60
TGTTCAAACA GGAGGCCCTG GCTGGCCGCA GCGACTCACG CCTATAATCC CAGCACACTG 120
GGATCAGAAG GATTGCTTGG GGCCAGGAGT TCCAGGAGTT TCAGGCCAGC CTGGGCAATA 180
CGGTGAGACC CCATCTCTAC GAGAAAGTTT CAAAAAATGA GCTGGGCATG GTGGCGCGCG 240
CCTGCAGTCC CAGTTACTCA GGAGGCTGAG GCAGGAGGAT CGCTGGAACC TGGGAGGCGG 300
AGGCTGAAGT GAGCTATGAT GGCGCGCCAC TGCCCTCCAG CCTGGGCAAC AGAGTGAGAC 360
CCTGCCTCAA ACAAAAACGT AAACAAAACA GGAGGCCCTG CTCTCCTGAG GGGCTGGTGG 420
TGAGTCACTG GTAGATGGGA GAGAGCTGGG GTCAGGGTCC CAGCTGGGGG GGTGGGTCCT 480
CACCTGTGCT ACCCTCCAGG GGGCCTCTCT CCAGGCCTCT GTCCCTCCCC TGGGAAGCCT 540
GGCAGAAACC TGAGACTGGG CCTCCAGTTC CAGGTCGCCA CTGGGCCCAG GCCTCTCCTG 600
TCCGCCTGCC AGGGACTGCG GAACAGGTAA CTCCTGCGCC ACCCTAAACC CACCTGGCCT 660
GTTGCTCCAG GTGCGGCCTG GAGGCCCCGG GGCCTGCACA CCTGGTCAGC TCAGAGGCCA 720
GGAAGAGGAG CGGAGGGAGG GGTGGGGCCG CCGGCCGCTG CTGGTTTCGT TTTGAGCCGG 780
GCCCCTTCTT CCTCCCTCCC TCCCACTCCT CGCCAGACCC CTGCATTCTG GGAAAGGCTG 840
TGACAACTTC CTCTGAACTC TCCTTAACCT GCCCTGGAGC CCAGGGCCTC CAGGAGGCTG 900
AGTTCCGCCT GCGGGACCTG AGGCTTCCTG CAGGTCACAC ACCTCCACCC CTGGCCACGT 960
GGCCCTAGAC CGCCCACCTT CTAGAAGCTT CTTTATGTGC TGCCCCATCA TGTCCCCACC 1020
CCGGGTGCAG CTGTCCCCTG CCTGCACCCC CTCCACCCTG TGTCCCAGAC TCTGCACACA 1080
GGAAACCGCC CTGGCCCCAG GGAGGGCTGC CTGAGACCCC CGCCTCCAAC CTGCACTGGG 1140
GACATCTGGG CTGGATGGTC CTCGGGAGGT GGGGCTGCCT TGGGCACTGC AGGGTGCTGG 1200
GTGACATCTC TGGCCTCCAT CCATTCCATG GCAGGGGCAC CCCCTGTCTC GACAACCACA 1260
GACGTCTGGG AGTTTCCAAG CCTCCCCTGG GTGGGGGGAC AGAATTGTTC CTGCTAAGAT 1320
CCAGTGGATT AAAAGACATC TGTGAGGGGA CAGAAATGAC TGAGTTTTGT GCCGGCCGGT 1380
CAGGCAGTCC CTGGCAGACA AAATTCCCAA GTATTTGCAT CCAAAAAAAC AAAACAAAAC 1440
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