| Tag | Content |
|---|
EnhancerAtlas ID | HS003-43802 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr8:22065950-22066950 |
Target genes | | Number: 25 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr8:22066349-22066370 | TTCCCTCTCCCCACCTCCTCT | - | 6.24 | | ZNF263 | MA0528.1 | chr8:22066346-22066367 | TCCTTCCCTCTCCCCACCTCC | - | 6.49 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27590 | chr8:22066597-22070769 | Esophagus | | SE_28211 | chr8:22066115-22071235 | Fetal_Intestine | | SE_29206 | chr8:22065809-22070849 | Fetal_Intestine_Large | | SE_35070 | chr8:22065703-22070846 | HeLa |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I022208 | chr8 | 22065726 | 22071201 |
|
Enhancer Sequence | CAGGCACCGC CCGTGACAGC ATGAGCCCAA GCGGGAGCCA GGCAGGAAGA AAGGCACCCC 60
GGCCTAACTG GGCATGTGTT GGTAGAGGCA TTCGAGGCAG GGGGAGGTGC CCAGGCAGAG 120
ACACAACCCC AGCCCAGCCC AGAGTGTGCC CAGGTGACAG CAGGTCATTT ACTTTGGCCG 180
AAGCAATGGG TGTGTGAGGA CAGCAGGTTG TGGGAATGAT GTGGCTGCAG AGAAAGGCTG 240
GAGTCCAGGG GGATGCCTTG AGTGCCAGAC CAAGGATGCC ACGAGGGAGC TTTGCAGTCT 300
CCTCCTGGGT CCTAAGCCAC CTGTCAGGGC ATCCCCAGAG CTGATGGTCC ACAGCCTCCC 360
CTCTTCCCCT TCAACTCAGT CCCTGACCCA GCCCCGTCCT TCCCTCTCCC CACCTCCTCT 420
AGCGAGACCT GAGTGCCAGG TGCACAAAAG CCAGAGGGCC TGGGGAGGAG GGTGGCCCCA 480
TGCACTGTCC TCTGCCCTTC CCAGCACAGG GTCACAAACC GGAGGCCCGG AACTCCATCT 540
GGCCCTCAGA CCTGCTATGT TTGGCCCACA CTGTGTTTTT TTTAAAAATG TGAGCCAACA 600
CTTAAAAGTT AGGAGTTTTC ACATAAAACC CAGATGTACG GCTTCTCTCT TGAAAATGGA 660
AGCTGTGGCG ACACTGGGCC CACATTCTTC CATGACAGCC ATCAGCTGGA GAAAATGAGC 720
AATGCCCTCT TTAGACAAAG TGTGTGGTGC CTCGTGCCAC CGCTCCATGC TGTCTTCCTC 780
TCGGTGAGCC TCACTGCCTG TTCCCCTCAG CCTAGGGCCA AGGTCCCTCT ATTTAGAGAT 840
GGGGCAGCAC AGCAATGTTC TGGGCCAGGC CCCCACCCAC CCATCACTGG CCTCGTGGCC 900
TTCACCCAGG CCTCCATCCT GCCGTGAGGG CACGCCATGG CATAGTGTGC CATGGGGCCT 960
GGCACCTGCG GTGCTCAGGG CTGGTTGGCC CCTCTTGTCC 1000
|
