| Tag | Content |
|---|
EnhancerAtlas ID | HS187-11227 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr18:3051640-3052820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr18:3052419-3052433 | TGATGACGTGGCCT | - | 6.6 | | ZNF263 | MA0528.1 | chr18:3052626-3052647 | TCCCCTCCTCCCTCTTCCTCA | - | 6.75 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_28141 | chr18:3050276-3054022 | Fetal_Intestine | | SE_29078 | chr18:3050099-3054070 | Fetal_Intestine_Large | | SE_31871 | chr18:3050831-3053355 | Gastric | | SE_35427 | chr18:3050253-3054042 | HepG2 | | SE_53034 | chr18:3050886-3053546 | Small_Intestine |
|
| | 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 |
| GH18I003050 | chr18 | 3050328 | 3053885 |
|
Enhancer Sequence | GAAAATAGTC TTTGAAATCT CAAACTTAAG CATTCCACTG TCTGACCATA ATATCCTCTG 60
GCCTGCTTAC CCAAAAGCTT AAATTCCAAA TATTCCTCTC TCATCGGGAC TACCAGTTTA 120
TTGAGCATCA TTTATCAAAT GTTCTTCTGA TTCTTCTTAC CCAGCCTTAG ACTCCAAGGT 180
CCAACACTAT AATCACTTCC TTGAGAACCA CCCTTGGCCA GACACAGTGA CTCATACCTA 240
TAATCCCAGC ACTTCGGGAG GCCGAGGTGG GCAGATCACT TGAGATCAGG AGTTTAAGAC 300
CAGCCTGGCC AACAGGCGAA ACCCCATGTC TTCTAAAAAA ATACAAAGAT TAGCTGGTTT 360
TGGTGACGTG TGCCTGTAGT CCAGCTACTT GGGAGGTTGA GGCACAAGAA TTGCTTGAAC 420
CCCGGAGGTG GAGGTTGCAA TGAGCCAAGA TCCTGCCACT GCACTCCAGC CTGGGTGACA 480
GGGCAAGACT CTGTATCAAA AAAAAAAAAA AAACCACCCC GACTTTGTTC CTTTGTTCTC 540
TCTCCATTTG TTTACCTACC TGACACAGCC CCGTCCTTCA GCATAACCAC ACTTGTGCAA 600
ATGAATGTTG CAGATAATTG CACAATGGTG CCACTAATGT GAAACATAGA TTTCAAATGG 660
ACTCTGGCAC TTCCTGGAAA CCTCTCACAT CCCCCTGCTC TCTAAGATAT TTATATCATG 720
CCTTTTCCTC TCTCCACTTA CCTCATTTTC CATCTTCCTC TTAATTATTC ACTCTCAACT 780
GATGACGTGG CCTCATAATT CCTTAAGAAT ATGGAAACAG AAAGGAACGT CCTCATCATC 840
TCACCATTAA CCACCTGTAT CTGTGCTCAT GTTCTTGCCT CCTGTCCTAT GAAGGTAGAG 900
GGTAAGTGTC CTCACCCAAG CACAGATGAA CCCCACCTGT CCTCTGAATG TCACCCTTTC 960
TTGTCTCCTG AGATCTGTCT GCATTGTCCC CTCCTCCCTC TTCCTCAGTC AGTCTCATCA 1020
GCATCTTCTA ATCTATCACC TGTCATCCTA AAGTCCCCCA CCCTACACTG AGTTCCCTTC 1080
AGCTACCATC TCATTTCTTT ACTCCCCAGT CAAAAAAAAA CTACTGGAAA TCATTATCTG 1140
TGCTCTGTGT CCCATTTTTC CTTTCTTTCT TTTTTTTCTT 1180
|
