| Tag | Content |
|---|
EnhancerAtlas ID | HS013-00145 |
Organism | Homo sapiens |
Tissue/cell | Calu-3 |
Coordinate | chr20:49377040-49378250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr20:49377766-49377776 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr20:49377766-49377776 | GGCACGTGCC | - | 6.02 | | ZEB1 | MA0103.3 | chr20:49377171-49377182 | GGGCAGGTGGG | - | 6.14 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_28210 | chr20:49377578-49379311 | Fetal_Intestine | | SE_29029 | chr20:49377430-49379871 | Fetal_Intestine_Large | | SE_31994 | chr20:49377044-49377793 | Gastric | | SE_31994 | chr20:49377826-49380492 | Gastric | | SE_36371 | chr20:49376947-49380175 | HMEC | | SE_43383 | chr20:49372403-49381684 | MCF-7 | | SE_47109 | chr20:49372782-49389800 | Panc1 |
|
| | 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 |
| GH20I050757 | chr20 | 49373714 | 49381510 |
|
Enhancer Sequence | AAATGCAATA TAAACTTCAA TCTGAAATGG CAGTTTCAAA TCCTATTACT TTCAAAGTAT 60
AGAAATGATA GGACCATGGG TCTCAGAGAG GAGGTTGCAA ATTCAAATGC CCAAAGGGCC 120
AGAGTGGGGC AGGGCAGGTG GGGCTGGTAA ACAGGAGATG CCCGCCCCCA GCAAGGCAGG 180
GGCCACCACA TTCGATGGTT GTCATTTGGG TATGTGTGGG CCCAGTGTTG TCAGCTCTTA 240
TAACTTTTTT TTTTTTTTTT TTGAGACTGA GTTTTGCTCT TGTTGCCCAG GCTGGAGTGC 300
AATGGCACAA TCTTGGCTCA CCGCAACCTC TGCCTCCCAG CTTCAAGCGA TTCTCCTGCC 360
TCAGCCTCCC AAGTAGCTGG GATTACAGGC ATCTGCAACC ATGCCCGGCT AATTTTTTGT 420
ATTTTTAGTA GAGATGGAAT TTCACCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTG 480
AGGTGATCCA CCTGCCTCAG CCTACCAAAG TGCTGGGATT ACAGGCGTGA GCCACCACGC 540
CCGGCCCTGC TTATCCAGAT TTTCATAAGA AATGTCCTTT TTTTTTTTTT TTTTTTTTTT 600
TGAGACGGAG TCTCGTTCTT CTGCCCTGGC TGGAGTGCAG TGGCAAGATC TTGGGCTCAC 660
TGCAACCTCT GCCTCCTGGG TTCAAGCACT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG 720
ACTACAGGCA CGTGCCACCA CGCCCAGCTA ATTTTTGTAT TTTTAGTAGA GACGGGCTTT 780
CACCATGTTG GCCAGGATGG TCTCAATCTC TTGATCTCGT GATCCGTCCA CCTCGGCCTC 840
CCAAAGTGCT GGGATTACAG GCATGAGCCA CCGCTCCTGG CCGAGAATCC CCCTTCCTAA 900
ATTGGTAAAA TCTGATTCAT CAGAATTGCA ATTTTGATCA AAGCCAGTAA CTCCTCACAC 960
AAATCCTTCT ATGTGTGCAG AAAGTGAGCG TCTGAAAACT CCAGGCGGAG TTTTTGCGCT 1020
AGGTTATCTA CCAGAAGAAA GGACAAGAAA GGCTAGAATT TGACTAATGG TTCCACCCCC 1080
CAGATTGTAT CAGCACAGCA TTCCTCTTTC ACTCAGTCTC TTAGCAATGC TTGCAACTAC 1140
AAGGAAACAG CATTCATACC ATTGTTTCTA AGACCTGAAG CAGGTTACAT TCAAACCCAG 1200
CACTGTTCTT 1210
|
