| Tag | Content |
|---|
EnhancerAtlas ID | HS040-01888 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:65382720-65383880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox6 | MA0515.1 | chr1:65382743-65382753 | AAAACAATGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_00278 | chr1:65380890-65384708 | Adipose_Nuclei | | SE_11209 | chr1:65382192-65384963 | CD20 | | SE_18759 | chr1:65382648-65384684 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_46185 | chr1:65380780-65384638 | Osteoblasts | | SE_68015 | chr1:65352732-65400925 | TC32 | | SE_68419 | chr1:65353166-65432877 | TC71 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 65382737 | 65382834 | | chr1 | 65383044 | 65383557 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I064914 | chr1 | 65380582 | 65384512 |
|
Enhancer Sequence | TTGCCAGGTT GGAAAGGCCC ATCAAAACAA TGGAGAAAAA GACCTGTTTG GGGCATTCCT 60
GGGAAATTTC ATAACATTGG AAACAAGGGT CTATAAAGCT TCCAAAAGAG AATAAAACAG 120
GCTACATTCA AAAGATCAAA AATTGAGAAT ATTCTCAGGC TTTTTAACAG CTGCACCAAG 180
GAAAGAGACA GGCACCCAAT GCCTGCAAAA TTCTGAAGGG AAACAACTTC CAACCCAGAA 240
GTCTATAACC AGCCAAATTA TCAACGAAGT ATGAAGGAAG AATCAAGATA CAGTTAGACA 300
TCAAAGATCT CAAAAAACAA ACTGCTATGC ATCCTTCTGA AAATAACAGG AGACAGGCTC 360
CAACACAGGA AATAAAGATT AAACAAAGAG GAAGTGAAGG GAACTCCCAG GAGCACAGAA 420
CAGAGCGGTC TCAACACAAA AGCTGTGGCC AGCCTCAGAG GATGACCAAT CCCCATGTGA 480
GCAGGGCAAC TTGAGGGATA CTTATGTTGA GGGCAGTCAC TGCCAAGATC CCCGTAGACT 540
GCATTGAGGG TAGAATGCCT GGGTGAGCCT GGACCAAATT CCTAATGGAA TTTGGTTTTT 600
CTTAATCATG CACTGATGAA ATTCCTGTTC CCCTGCTGTG TCCTGCTGCC TGAATCAGCA 660
GAAGACTATT TCACCCCGCA GAAGTATTCC ATTTGGCCTA TTCCTGAGAG CTGGACATAA 720
GCCAGGGTGG AGCAGCACAT TCCTCTTGAC TCCACTCCTC CCAGGCTCCC AACAGCTGGG 780
CCCACTGCAG TCTTCTAGGT ACCTCCAACT ATGAGAAGCC CTGTTTCCCA CAACTCATTC 840
ATGATCTTTT CCACTGACTT TCCCAAAAGG GTCCCTGCAA CCTCTCAACT CTGGATCCAG 900
ACTTGACCCA GAGTTTCTGT TCAGACACAG GGGTAATGAA TTCAACCAGA GACCATGAAG 960
CTCTTCTCCT GGGAGCCTTC ATCTAGAGAT GGCATCACTG CCCTTTCCTT ATACACCTAG 1020
GTTTATGCTT GCTCTGGGGA CATATACACT GGTAGAAAGG GCATGATTAA TACCAAAGTG 1080
GGGGTGACTG TTACCTCTGA GGGAAGTGCA GTGGAGGGGA CTACCAGGTG ATTTCTAAGA 1140
TACCAGTAAT GTTCTCTTTC 1160
|
