| Tag | Content |
|---|
EnhancerAtlas ID | HS040-17913 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr19:11009040-11010400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr19:11010306-11010317 | TGGGTGTGGCC | - | 6.62 | | TFAP2A | MA0003.3 | chr19:11009971-11009982 | CGCCTCAGGCA | + | 6.62 | | ZNF263 | MA0528.1 | chr19:11009517-11009538 | GAGGGAGGGGAGAGGAAGGGA | + | 6.22 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23673 | chr19:11008924-11010460 | Colon_Crypt_1 | | SE_24532 | chr19:11008947-11010425 | Colon_Crypt_2 | | SE_30825 | chr19:11008999-11010458 | Fetal_Muscle | | SE_48197 | chr19:11008793-11011250 | Psoas_Muscle | | SE_51520 | chr19:11008746-11011610 | Skeletal_Muscle | | SE_68858 | chr19:11008941-11010261 | H9 |
|
| | 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 |
| GH19I010898 | chr19 | 11009109 | 11010781 |
|
Enhancer Sequence | CTCCTGGCTC TAGAGTCTGC TTTTTGGTCA CCCTTGCCTG CTAGCCCTGC AGCCTGTCCC 60
CCACCTCTCC AGGCCATGTG CACACAGTCC CCAACATGCG CCGGCTGATG CCGCAACAGT 120
GGTGCTTTTT GGATTTGTCT CTAGAGGCCA ACACAGAGGG CCTTTCTGAA TCCTGGGGTC 180
CTGCCCCCTT CCGCGGCTCC CATACTGCTC CTCCCCAGCT GAATGGCCGC TTTGGGAGGT 240
GGTTGCTGGC CTTGAGAGGA TGCCACAGTG AGTTTCCTGC GGGCAGGGCT GCATCTGTGG 300
CGAGCACTGA ATCGCCACTG CTGGATCCAG ATGCCTGTGC GTCCCGGGCC CCAAGGCTCC 360
CTTCTACCCT CCTCCTGGGG TGCTGTTCGC AAGCCAGGAG ACAGGCTGTG CATTCCCTGC 420
CTACTCAGAG GTGACCCTGG GCCAGGTGTG CGATGGCCCA CTGGACCCAT AGTAGCAGAG 480
GGAGGGGAGA GGAAGGGAGA AAGTGGGAAC AGCATGTGCA GAGGCCTGGG GCCTGGCCCA 540
TGTAGGGACT AGAGGGTTGA GTGTGTCCAT GGGGAGGGGC CAAGACGGGG AGAGCCATGA 600
GGAATGATGG GCACAGAGCT CAGAGGCTCG GGAGTCTCCT GAACAAAGAG AGGAACACGG 660
CTTAGCTTGT TTTTTTTTTT TTTTTTTTTG GTTTGTCAGT ATTTCCCAGG TGTCTTCTGT 720
GTGCCAGGGA CTAACTTGGG GATAAAGCTG TGACTTTGAG AAGCTGCCGG CTCCGCGGGC 780
TTTAGCAGCT GCTGCTGTGA TGAAGCGATC CACTTGCCCT CAGCCCCGGC ATCTTTGGCC 840
CAAGCCCAGC CCTAGCCCTG GCTGGGCACA GCCAGGCTTC ACTTGGCCAC AGGTCCTGTA 900
GTTGCCTGCC TGGCGCCAGG TCAGAGAGGG ACGCCTCAGG CAACATCGGG TTGCCAGGCT 960
GCTTGGTAAA CAGGCCTCCC TGGGCCCACT TGCTGTCGCC CAGGTGTGGC TAACAGATCG 1020
ACAGTATCTC CTGCCCCAGG ACGGGTATGA GTGTGGGCAC CATGCCAAGG TTGGATGTCC 1080
CTTCCTGGGA CCCACCCACA GCTGGGAGCA CTTTATCTTG GGCCTCTGTG GGTGTAGTGA 1140
GGCTGTGAGT CTGGGGCAGT GGCCTGCTGA CACCCTCCTG GCAGGGCTCA GGAGGTTCCT 1200
CCATGCCCTG CCCTCAGGAG GGCGGCACCT GGCTCCTGGG GTGGGAGAGA GTCTGGCAGG 1260
ACTGGCTGGG TGTGGCCGGG GAGCTGCCCT TCAGGTCTCA TATCTGTAGG CCCTCATACC 1320
TGGACTCGTC AGTTAGGAAC AGTTTTCTTT TTCTTTTTCT 1360
|
