| Tag | Content |
|---|
EnhancerAtlas ID | HS076-53198 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr8:22065960-22066950 |
Target genes | | Number: 16 | 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 | CCGTGACAGC ATGAGCCCAA GCGGGAGCCA GGCAGGAAGA AAGGCACCCC GGCCTAACTG 60
GGCATGTGTT GGTAGAGGCA TTCGAGGCAG GGGGAGGTGC CCAGGCAGAG ACACAACCCC 120
AGCCCAGCCC AGAGTGTGCC CAGGTGACAG CAGGTCATTT ACTTTGGCCG AAGCAATGGG 180
TGTGTGAGGA CAGCAGGTTG TGGGAATGAT GTGGCTGCAG AGAAAGGCTG GAGTCCAGGG 240
GGATGCCTTG AGTGCCAGAC CAAGGATGCC ACGAGGGAGC TTTGCAGTCT CCTCCTGGGT 300
CCTAAGCCAC CTGTCAGGGC ATCCCCAGAG CTGATGGTCC ACAGCCTCCC CTCTTCCCCT 360
TCAACTCAGT CCCTGACCCA GCCCCGTCCT TCCCTCTCCC CACCTCCTCT AGCGAGACCT 420
GAGTGCCAGG TGCACAAAAG CCAGAGGGCC TGGGGAGGAG GGTGGCCCCA TGCACTGTCC 480
TCTGCCCTTC CCAGCACAGG GTCACAAACC GGAGGCCCGG AACTCCATCT GGCCCTCAGA 540
CCTGCTATGT TTGGCCCACA CTGTGTTTTT TTTAAAAATG TGAGCCAACA CTTAAAAGTT 600
AGGAGTTTTC ACATAAAACC CAGATGTACG GCTTCTCTCT TGAAAATGGA AGCTGTGGCG 660
ACACTGGGCC CACATTCTTC CATGACAGCC ATCAGCTGGA GAAAATGAGC AATGCCCTCT 720
TTAGACAAAG TGTGTGGTGC CTCGTGCCAC CGCTCCATGC TGTCTTCCTC TCGGTGAGCC 780
TCACTGCCTG TTCCCCTCAG CCTAGGGCCA AGGTCCCTCT ATTTAGAGAT GGGGCAGCAC 840
AGCAATGTTC TGGGCCAGGC CCCCACCCAC CCATCACTGG CCTCGTGGCC TTCACCCAGG 900
CCTCCATCCT GCCGTGAGGG CACGCCATGG CATAGTGTGC CATGGGGCCT GGCACCTGCG 960
GTGCTCAGGG CTGGTTGGCC CCTCTTGTCC 990
|
