| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00100 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:2225570-2226400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr1:2226337-2226351 | GGCCACGCCCACCC | + | 6.69 | | Klf12 | MA0742.1 | chr1:2226337-2226352 | GGCCACGCCCACCCA | + | 6.28 | | SP1 | MA0079.4 | chr1:2226335-2226350 | GAGGCCACGCCCACC | + | 7.19 | | SP3 | MA0746.2 | chr1:2226337-2226350 | GGCCACGCCCACC | + | 7.52 | | SP4 | MA0685.1 | chr1:2226335-2226352 | GAGGCCACGCCCACCCA | + | 6.8 | | SP8 | MA0747.1 | chr1:2226338-2226350 | GCCACGCCCACC | + | 6.62 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_11303 | chr1:2225203-2227097 | CD20 | | SE_17322 | chr1:2224537-2236334 | CD4p_CD25-_CD45RAp_Naive | | SE_18345 | chr1:2225163-2227486 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19191 | chr1:2225604-2226867 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_46124 | chr1:2225104-2226854 | Osteoblasts | | SE_68719 | chr1:2225251-2226430 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I002295 | chr1 | 2225640 | 2225839 | | GH01I002294 | chr1 | 2225921 | 2226070 |
|
Enhancer Sequence | CAGCTTCCTC TTCCCCTGAG CGGGGGCTTC CAGAGCCTCC CTCCCACTGG TGCCCATGGG 60
GTTTGAGCCT GATAGCTCCG CAGGATTCAG CTGCTGTGAG TCACAGCCAG GATGGAGAGG 120
TCTAAGGCAG GCCTGATGCC GGGCAGGGCG ACATTTCTAG AAAAGGTTTC ATCTGGTGAT 180
CTGCTAAATG GCATGAAAAT CACAAAATTG GCACTCAGTG ACCATCAGGC TGGCTGTGTG 240
TGGCTGCTCT CCTCAACAAG CAAATGGCTG CCCCCATCCA GAGCCCCGAC TCCCGCTGGC 300
CTCCCCCGTG CGGGGATGTG GGGACCAGGG CAGGCCCCAG AGACCACCTG ACCTCTCTGG 360
CAGGAAGAAG ACCACGTCGT GCCGTTTCCT CCTCCCTTGA GCCCGTTAGC TGTCTCGGGG 420
AACCGGTAAG CCCAGGGCCA CCTTGTCACG TCCTCCACTG AACGTGGGTC CACGTAGATG 480
CCAGCCCCTT GGTCTTGCCC AGAAGTTGTG GGAGGTGCTG GTTGCCAGGG ATGGCTATGC 540
ATGTTTGTCC CCATGGCAGG GAGGCCTCTG GGGGCCTGGC CCTCCCCCCG CTAGCTGCTT 600
CTCACATTTT TGTCTCCCCG AGAGCCACCT GCTCTCCCAG GGCCCTCAGG CCCCCGTCTG 660
CCAGTCTCCT GGCACCTGGG CTGGGGTCTG CGCCAGGCAA CTCCCACAGC AGGGCAGGAT 720
CCACCCTCCA CGTTATCATT ACTGCCATCC CCTGTGCCTG GGTTGGAGGC CACGCCCACC 780
CAGTGGGGCC CCTCTGGAAA GGAGACTTGA CCTCAGGGTG GTGGCAGGGC 830
|
