| Tag | Content |
|---|
EnhancerAtlas ID | HS040-02571 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:159910860-159911980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr1:159911606-159911616 | GCTAATTGGG | - | 6.02 | | ZNF263 | MA0528.1 | chr1:159911451-159911472 | CCTCCCTCTTCCACCTCCCCT | - | 6.37 | | ZNF263 | MA0528.1 | chr1:159911448-159911469 | GCCCCTCCCTCTTCCACCTCC | - | 6.42 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28185 | chr1:159905613-159916500 | Fetal_Intestine | | SE_29354 | chr1:159905717-159916603 | Fetal_Intestine_Large | | SE_63399 | chr1:159883649-159916570 | NCI-H69 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 159911000 | 159911546 | | chr1 | 159911680 | 159911946 |
|
Enhancer Sequence | CCATGGCATC GTTGATAAAT CCAGTCTCCT CTACTAGATG CTTCTAGAGT CCTCAAAGAT 60
GGGAAGCCTT CCCTTCTGTG TGGTCCCTAA TCCAACAGTC TCTCTCAGGG TTCCGCACAC 120
ATTCTAGGCC ACCAGCCCCA CAACAGTCCC CGACCCATCT CCCCTTCACT GCCCAGAGGG 180
CTTATGACAG AAGAGCATTG TCCTTAGCAA CCTCTACCTC CTGTTGCTTA GCAACTGCAG 240
TTCCGAGTCC CCTACACAAA GGCTGAGAGG CCCCTTCCAC ACTGTGAGGC AGTAAAAGGG 300
TTAATGGGCT CAGGGGCCTC CCTCAGGTCC CAACTCCCTC AGCCGGCTCT GGCCTGACCA 360
AGAGCTCCAG ACGGAGGTAG GGGTGTGAAC AAAGGATAGG AGCAGACAGT AAGTCCCAGA 420
GGCTACTGCT CACAGCCCCT GTAGCTCAAG CAACAGCACA GACAGAAGAC CCACAGGTAG 480
ACAAAGTTGC TAACCATCCA GTGGCTTCAG GCCTGAGGGA CCTCAAGGCA GGACACAAGC 540
TGGAGAGAAG GAAGAGCTTC AAGTCTCCCT GGTGGAGTCC CAGGAAAAGC CCCTCCCTCT 600
TCCACCTCCC CTTGCCTTGC CCTCAGTCAG GCAACATTAT GAATCTGTCC AGCCTCAGCC 660
CGGCAGCCCG AGACCCCTCC CAGGCCTGGG CAGGCGGAGG CAGGGAGGGA GGGCTGGTGG 720
GCACAGCCGT TTTTTTCTCC ACTGGTGCTA ATTGGGGCCC GCTTTCATCC ATTCCCACAG 780
GGCTTGTGTA GACACATACA CTCCCACCAG GCTGTTTGCC AATAACTGCC CCCAGTTTGA 840
AAAGAAACTT CCCTTCTGCA TCACCTGCCT GCACCTCCTC CCCTCTCTGC TCAGCCCGCC 900
CTGTGGCAAG GCTCAGCCAA TCCCGGGGTT TCCCTCAGGA TTCAAACTAA AGAGGGAAAA 960
GGTGGGGGTC TCCCCATCAA CATCCTCCCA GGTGGCCTTT CCTGGGTCTC CCCTCTGAAG 1020
AGGAGGCAAC AAGACTCTCT CTCGCCCCAT AGCCCAGACC TGTCCTTAGG GCCTCCTGCA 1080
GACTGCCCTC TGAGACCTGG CACTAAACCG CTTAGATTAA 1120
|
