| Tag | Content |
|---|
EnhancerAtlas ID | HS023-12189 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr19:4082770-4085360 |
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: 21 | 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 | chr19:4082893-4083451 | Colon_Crypt_3 | | 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 | AACCTGGGAG GCAGAGCTTG CAGTGAGCCG AGATTGCGCC ACTGCACTCC AGCCTGGGTG 60
ACAGAGCGAG ACTCCATCTC AAAAAAAAAA AAAAAAAAAA AAAAAAGCTG CCCCCCTTTC 120
TTGCCTGGAG GGAGGAAGGG ATCTCAGCTT CATGGCCATA TTTTGAACCT CGTTGCTCCC 180
AGCCCGCGCC CCCAGCCAGG CTGGGCCTCT CCAAGGGCCC CTGTCACCCA GTCCTGCCAC 240
CCAGCCTTTG CTGACACCGT TGCCCATGTT GGCCCCGCCA CTGTTGGGAA TGTCCTCTCC 300
AGCCCTCAGC TGTGGATTCC CCTCCTTCCC AGGACTTCTC CTCTAGGTGC TGGCTAAATT 360
TGCCTTTAGC CCTTAGGGCG GCTATAAATT CTAATTTCTG GGCCCGAGCG AGCGCCGTGG 420
GGAGGCTGCA GGCTCCCCAG CGATGGACAG GGGCTCTTAT CTTTTAGGAT CCCACAGAGC 480
ACTGCAGAAA AGCCCCAAAT ATTTGTGGGT CACGAAGGCA GTGTCCTGTC AGGGGAGACA 540
GCAGGATGGT GGGACCACAG GATCGTCCAT GTCTTCCCTG GGGGAGGTTC GAGTCACCTT 600
CAGAAGGTCA CCTAACTTGC AGGGACTCCG CTGCCGCAGA GGTTGTGTGG GGAGAGGCAA 660
ACCTGGTCAG CCTATTTTGT GGGGTGCAAA CAGAAGGGAT GTGGGCCTCC TCGGAAGTCT 720
GCAGAGAGGA TTCGCTCCTC CGTGGACGCT TCTCTCTTTT CTTGAGCCTG TGATGAGTTC 780
CTTTGCAAAT AGGGAAACTG AGGCTCTCAG AGGGGATTCT ATCTTCCCCA AGGTCACAGG 840
CCCAAGGACA GCAGAAATAT CGTCAGGCCT GTGGTCCTGA TGTTCAAACA GGAGGCCCTG 900
GCTGGCCGCA GCGACTCACG CCTATAATCC CAGCACACTG GGATCAGAAG GATTGCTTGG 960
GGCCAGGAGT TCCAGGAGTT TCAGGCCAGC CTGGGCAATA CGGTGAGACC CCATCTCTAC 1020
GAGAAAGTTT CAAAAAATGA GCTGGGCATG GTGGCGCGCG CCTGCAGTCC CAGTTACTCA 1080
GGAGGCTGAG GCAGGAGGAT CGCTGGAACC TGGGAGGCGG AGGCTGAAGT GAGCTATGAT 1140
GGCGCGCCAC TGCCCTCCAG CCTGGGCAAC AGAGTGAGAC CCTGCCTCAA ACAAAAACGT 1200
AAACAAAACA GGAGGCCCTG CTCTCCTGAG GGGCTGGTGG TGAGTCACTG GTAGATGGGA 1260
GAGAGCTGGG GTCAGGGTCC CAGCTGGGGG GGTGGGTCCT CACCTGTGCT ACCCTCCAGG 1320
GGGCCTCTCT CCAGGCCTCT GTCCCTCCCC TGGGAAGCCT GGCAGAAACC TGAGACTGGG 1380
CCTCCAGTTC CAGGTCGCCA CTGGGCCCAG GCCTCTCCTG TCCGCCTGCC AGGGACTGCG 1440
GAACAGGTAA CTCCTGCGCC ACCCTAAACC CACCTGGCCT GTTGCTCCAG GTGCGGCCTG 1500
GAGGCCCCGG GGCCTGCACA CCTGGTCAGC TCAGAGGCCA GGAAGAGGAG CGGAGGGAGG 1560
GGTGGGGCCG CCGGCCGCTG CTGGTTTCGT TTTGAGCCGG GCCCCTTCTT CCTCCCTCCC 1620
TCCCACTCCT CGCCAGACCC CTGCATTCTG GGAAAGGCTG TGACAACTTC CTCTGAACTC 1680
TCCTTAACCT GCCCTGGAGC CCAGGGCCTC CAGGAGGCTG AGTTCCGCCT GCGGGACCTG 1740
AGGCTTCCTG CAGGTCACAC ACCTCCACCC CTGGCCACGT GGCCCTAGAC CGCCCACCTT 1800
CTAGAAGCTT CTTTATGTGC TGCCCCATCA TGTCCCCACC CCGGGTGCAG CTGTCCCCTG 1860
CCTGCACCCC CTCCACCCTG TGTCCCAGAC TCTGCACACA GGAAACCGCC CTGGCCCCAG 1920
GGAGGGCTGC CTGAGACCCC CGCCTCCAAC CTGCACTGGG GACATCTGGG CTGGATGGTC 1980
CTCGGGAGGT GGGGCTGCCT TGGGCACTGC AGGGTGCTGG GTGACATCTC TGGCCTCCAT 2040
CCATTCCATG GCAGGGGCAC CCCCTGTCTC GACAACCACA GACGTCTGGG AGTTTCCAAG 2100
CCTCCCCTGG GTGGGGGGAC AGAATTGTTC CTGCTAAGAT CCAGTGGATT AAAAGACATC 2160
TGTGAGGGGA CAGAAATGAC TGAGTTTTGT GCCGGCCGGT CAGGCAGTCC CTGGCAGACA 2220
AAATTCCCAA GTATTTGCAT CCAAAAAAAC AAAACAAAAC AAAACAAAAC AAAACCACCC 2280
AGCGTGGTGG CTCACACCTG TCATCCTAGC ACTTTGGGAG GCCAAGGCGG TCAGATCATT 2340
GAAGTCAGGG GTTCGAGACC AGCCTGGCCA ACATGGTGAA ACCCTGTCTC TACTAAAAAT 2400
ACAAAAATTA GCCGGGTGTG GTGGCACATG CCTGTAATCC CAGCTACTCG GGAGACTGAG 2460
GCAGGAGAAT CGCTTGAACC CGGGAGGTGG AGGTTGTGGT GAGCCGAGAT CACGCCACTG 2520
CACTCCAGCC TGGGCAGCAA AGCGAGACTC CATCTCAAAA AAAAAAAAAA AAAGAGAGAA 2580
AAACCTAAAT 2590
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