| Tag | Content |
|---|
EnhancerAtlas ID | HS040-26879 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr4:1854600-1855380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr4:1855107-1855117 | ATCAAGGTCA | + | 6.02 | | ZNF263 | MA0528.1 | chr4:1854835-1854856 | CCCTCCTCATTCTGCTCCTCC | - | 7.52 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23339 | chr4:1852695-1855704 | Colon_Crypt_1 | | SE_23994 | chr4:1854600-1855445 | Colon_Crypt_2 | | SE_24875 | chr4:1854657-1855671 | Colon_Crypt_3 | | SE_30934 | chr4:1850182-1856054 | Fetal_Thymus | | SE_50496 | chr4:1852664-1855883 | Sigmoid_Colon |
|
| | 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 |
| GH04I001852 | chr4 | 1853882 | 1855411 |
|
Enhancer Sequence | TCCCATCATT CAGGAAACTT CCAGGGTTCT CAGCCCTCAG TGCTGGTGCC AGGATCAGGT 60
CAAAGAACAA ACAAACCTTT CTTCACCTGG CTTCACCCTT GCCACTCCTG GGAGAGCCTC 120
CCTACCTGAC CTCCACCTCC TCCCCAGGCA ATCTCTTCCC TGACTTGAAT ACACACGCCC 180
CACAGGTCTG ATGGGCACGG CACAGTCCAC ACCTCCAAGA ACTCTCAACT AGCGCCCCTC 240
CTCATTCTGC TCCTCCCCAA GTCCTCCCCA GTTTCAACAA ATGGCACTGT TGTCCCCAGG 300
CGGCTCAGGC CAGAGGCCAC CTCTCCCACA CAGCCCTCAC TGTTGTCCCC AGGCGGCTCA 360
GGCCAGAGGC CCCCTCTCCC ACACAGCCCT TGGAGTCAGC CCTGCTTCTG CTCGTAAAGC 420
GACTTCCTCC CAAAAAGGAC AAATGGGGAG GTGGGACAAG AGTAACTGGG CAGTGAAAAA 480
CCTGACAAAC ACCACTTCAG CCTACTGATC AAGGTCAACA TCAACAGTGA CAAATCATTT 540
GGACAGCATG GAGCCTCGGC GGGATATGAT AAGGATGCTT CACCTCTGTG GTCTTCCTCC 600
TGAAAAACCA TCTTTCCCAG CTTAATTATG AGGAAACATC AAGAAATACC AGTAGAGCAG 660
CACCCTACAC TCCACCTGGG CAGTACTCCT CAAAGCTGTC AAGGTCACTG CAGACAAGGA 720
AAGCCTGAGA GGCAATCAAG AAGGGTGGTA CAGATGGGTC CTGGGACAGA AAAAGGACCT 780
|
