| Tag | Content |
|---|
EnhancerAtlas ID | HS178-00398 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr1:17949670-17950880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr1:17950741-17950755 | GGTCCCAAGGGAGT | - | 6.15 | | ZNF263 | MA0528.1 | chr1:17950555-17950576 | TGCCCTTCTCCTCCCTCCACC | - | 6.22 | | ZNF263 | MA0528.1 | chr1:17950548-17950569 | TTCCCCCTGCCCTTCTCCTCC | - | 6.41 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_01537 | chr1:17947922-17953357 | Aorta | | SE_09560 | chr1:17949821-17964167 | CD14 | | SE_26573 | chr1:17950237-17952175 | Esophagus | | SE_40808 | chr1:17949037-17953149 | Left_Ventricle | | SE_49224 | chr1:17948837-17952605 | Right_Atrium | | SE_65277 | chr1:17948671-17950143 | Pancreatic_islets | | SE_65277 | chr1:17950412-17951739 | Pancreatic_islets |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I017621 | chr1 | 17948068 | 17950143 | | GH01I017624 | chr1 | 17950866 | 17952070 |
|
Enhancer Sequence | GTAAGTGTCC CCAAACTTTT TCCCCAGCCC ACCAAGGTAA AACCACAACC AGTCTGACCC 60
CGGGGCCATG CAGTCCAGCC TCCTGCCTCT GCCTGCTTGC CTTGTTCAAG TCAGTGGGAT 120
TAGAGGGTGG CAGGGTCTTC TGGGCCTGAT CTAGGGGTGA GTGTGACACC TTGAAGTGGC 180
CAGGATGTCC TTGGATATAC CTGGCAGGCC ATGGTGCTGA TGAAGCCAGG TGGCTGTCCT 240
GGCTCCTCCC AGGTGGCAGC ACCCCCTGGC CTCCCAGTCA CTGTGGGCAG CCACCTGGCC 300
GGTCACAAGC TCTCTTACCG AGCACTTGAG GGGTTTCAAG CCAGTGTGAA ATGCTGTGAA 360
AGACCACAAC TTTGGCCCGG AGAGGATGTG CCGCAGTGCT GGGGAAAGGG CACTGGCTCA 420
CGATCCGGGG GACCTGGTTC TGGTCCCAGC TCAGTTCTGC AACCTAGGGC AGGTCCAGGG 480
CCCACTCTGA GCCCAGGCTT GCCATCTGTG GAATGAGGGG TGCACTGGAT TTCTGGCTTT 540
TCTAGCTGAA GTCTGCGGAC CCCAGATGTT CATGGGGTGA GGGAAGGTCA AGTTGGTAGC 600
ACTCTACTTT GATGTGTTTT AGGTAACTAG GTTTTGCTAA AAGAAAAAAA CTTTTTTTTG 660
AAAGCCACAG CGCTCGATAG AGTCACTGAA TAGGTCTGAT GTTCTGGGTG TATATCAAGG 720
GGCTCTGGAG AGAGAGTTGA TTGACTCCAG GCCGACCATC CCTCCCTTGG TAACTCAACT 780
CTGGGCACGC TGCCCGGTGA GAGGCCAGGA GCACTTTCCT TAAAGGTGGA GGGCAAGGGG 840
CATTCGATTT CCTGAACGTG AATGCAGTAG AAGGGGTGTT CCCCCTGCCC TTCTCCTCCC 900
TCCACCTGTG GGCTTGGGCT GCTGCACTGG GGATGGAGAC CTGGGAGGCG AAGGTCCCCT 960
GGGCTCTCCT GTGGCACCAC CCCATCCCAC CTGTGACCTC AGGCCAGCCT CTCTACCTCT 1020
CTGAGCTCCA TGTCCACACC CCAGTGGGGG TGATGGATTT GCACAGCTCG AGGTCCCAAG 1080
GGAGTGTGGG GTGAGTGCAG GCGCCCTTCT GCTCCCTGCC TTGAGGCGGC CTCCCTGGCC 1140
CACACCTGCC TCGTTTCCTT CTGCTCCCTG CATTGAGGCG GTCTCCCTGG CCCACACCTG 1200
CCTTGTTTCA 1210
|
