| Tag | Content |
|---|
EnhancerAtlas ID | HS040-05022 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr10:98026180-98027080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr10:98026895-98026905 | AACATATGTC | + | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_10441 | chr10:98025976-98037587 | CD19_Primary | | SE_29175 | chr10:98026422-98033876 | Fetal_Intestine_Large | | SE_32567 | chr10:98026187-98034906 | GM12878 | | SE_58700 | chr10:97989552-98067150 | Ly1 | | SE_59131 | chr10:98023167-98051753 | Ly3 | | SE_60551 | chr10:97989174-98053492 | DHL6 | | SE_61310 | chr10:98026574-98059963 | HBL1 | | SE_62958 | chr10:98026186-98060541 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTCTGGTTT AGGGTTTTCC TAGCACAGCC ATGCCCAGAG TGGGTGAGGA AGTTGCCTTG 60
AGTTTTCTTG GCTGATGACT CTGAAGTCCA CTCGCACTAA GCCAGTTTCT GATAACGTGG 120
CTCCCATGTG ACTTGCCCAC AGGGAGAAAG AACCCTTCTC AGCTGCTCTG GGTAGTCCAT 180
CCATTGGTGT GCCGCAAGAT GGTCCAGTTA AGTGGCTTCT CATCCAGTGG GATGCAGGTA 240
GGCAGTGTGA GGGGATGGGA AACCAGACGG TCCAGGAAGT GGATCTAATC TCCACCACTA 300
GATGCTGTGC CTCCTGCCTG CAGCTCCCCT GAAGTTTGCC ACCCCAGTTA AAAGGAGTTG 360
GAACCACAAA TATGAAGAGC AAGAGAGACA GCAAATGCCA CTCAGCTTGG GTGGTTTGAG 420
GTACTGGTGG TTGTGTTTGC TTTTTATTGA CTTGGTATAC TGACTAAGTG GCAAATACTC 480
TTCTGGGAAC TTCAGTCCAT GTTGTCTCAC TTGGTCTTCA CACAAGCCTG TGAGGAAGGC 540
ATCTCTAGCT TCGTTTGGCA GCTGGGAAAA CTGAGGTGTA GAGAAACTGA ATGGCTTCAG 600
CTAGTAACTG GCCATTAGAA TCAGCCCTGT TGGGCCCCAA TGGCATGGTC CTTCTAAATA 660
TATCAAGAAA TATTTCCTGA GAGTCCTGAG ATAAAATGGT AGCCTTTGAG AATGTAACAT 720
ATGTCAAATG TGGTCTCTGT GCTTAAAGGA TCACAGCATC AGAGCTGAGA GGGACTTTGG 780
GAAATGTTCT CATTTTGTAG TTTGAACCAA ACAAACATAG GGGACATGGG GGAGCTAATA 840
ACCTATCCGG GATGTTGTGG AAGAAAAGGA AAGAAAAGCC ATATATGGAA GAGAAGAGCC 900
|
