| Tag | Content |
|---|
EnhancerAtlas ID | HS034-08813 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr14:35836440-35837620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr14:35837022-35837037 | TTCTATTTTTATCTT | - | 6.63 | | ZNF263 | MA0528.1 | chr14:35837151-35837172 | GCCCCCTCACCCGCCTCCTCC | - | 6.87 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_00565 | chr14:35836857-35838165 | Adipose_Nuclei | | SE_26613 | chr14:35834109-35836736 | Esophagus | | SE_27693 | chr14:35833874-35837755 | Fetal_Intestine | | SE_28626 | chr14:35833820-35837563 | Fetal_Intestine_Large | | SE_40331 | chr14:35833964-35838440 | K562 | | SE_42211 | chr14:35834222-35837002 | Lung | | SE_50091 | chr14:35834124-35838759 | Sigmoid_Colon | | SE_52425 | chr14:35834235-35836856 | Small_Intestine | | SE_53368 | chr14:35833998-35837726 | Spleen | | SE_56156 | chr14:35832346-35838097 | u87 | | SE_67556 | chr14:35832346-35838097 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I035364 | chr14 | 35833498 | 35839881 |
|
Enhancer Sequence | GGTGGAGGGG CCTGGCTACC TGTCTGCAAA TGTGGAGCCG GGGGAGGTTG GTTGGCAGAA 60
AGGAGGGAGA AGTGACGAGG CGCCCCAGGC CCTGTGCCTG GAGTCAGAAG GGCCAGCTCT 120
GGGAGAACCT TCACCCTCGT GGAGACTTTG CCTCAGAATG TTTGCCTGGA ACCCAGCCCA 180
CCAGGGCTGA CACCTGAGGC TGAGGCTGCC CTGTCATGCC CCTTCCACAC CAGGGGCTCT 240
GTGCTGGGAT TGCTGTGGCC AGTTACGGGG AGGCCTGCAA GTTTGGGCAG CCGAGGTCAT 300
GCCTCTCAAA GAGGAGCCGG ATGAATATAT CAAGTAAATG TGCATTTCAG CTTGTGGTAG 360
GGCCAGACAC AGCTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTAAGG 420
GGAGCAACAT TCACTGTGCA CCTACCATGT GGCAAGCTAG TGCTAGGCCC TGTACTTGTA 480
CTATTTCATT TAATGAGTTT AATTTGCATG GCTGCTTCTG TGGCATTCCA GAGTGGCTTT 540
TCACACTTTC TTTGGCTGGG GTGGGGGTGG GGAGAACTGT ATTTCTATTT TTATCTTCCC 600
ATGGTGGGGT GCTCTGCTCA TGGGGCCCCT TATCTCCCCC GGCACTTTCC CCTACATCCG 660
GCTGCAACTA GAAGCTTTCG GTATGCAAAG GGAACTTGCA GCTTCACAAC AGCCCCCTCA 720
CCCGCCTCCT CCCAGCCCTG CATGGGGGTC AGGCCACCTC TTCCCCAGGA GGACCCTTCT 780
TCTCTTCTGG GCTGGATGGA GGCAGGATCT GTGCTTCTCC CTCAAACCTG GGAACCAACT 840
GGGAGGGACA TCTTCTCCTT TCACCCTCTT GCCCCAGCAG CTCAGGGGTT CATTTGGATG 900
AATGGGCCCT GCCTGTAGCA GCCTGGCATG GGGGCAAACC AGGACTCCAC ATGGCTGAGG 960
AGCTCCCCGG GCCCCTGCAC TCCATTGGGT TGACTTATTT TAACCCATTG CACTCCCAGC 1020
TGAGCTTTAG AGGGCAAGGT TTGGGGTTAG TGGGTAGCCT TGGGGTTGGA GGTGCAGTCC 1080
CGCATAGTGA CTTGACATCT AGGAAGAGCT CATTGTTCTG AATGTGATCT TTACAACCAC 1140
CCTGAGGCTG GTCCCTAAAG CTATGCTCTG GAAATGAGTC 1180
|
