| Tag | Content |
|---|
EnhancerAtlas ID | HS156-04674 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr16:30092630-30093800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr16:30092929-30092939 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr16:30092929-30092939 | GGCACGTGCC | - | 6.02 | | IRF1 | MA0050.2 | chr16:30093377-30093398 | AAAAAAAAAAAGAAAGGAAAG | - | 6.2 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_31719 | chr16:30092037-30092861 | Gastric | | SE_35600 | chr16:30091964-30093106 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I030080 | chr16 | 30091965 | 30093106 |
|
Enhancer Sequence | AGTGAGTACC TGCTGTCCCT GCAGAGCCAG GCCTGGTCTT TCAGGCACAT GAAGTTTCCT 60
CTTCATCTTG GGGGCTCTAT AAGCCCAACC CTAAGCTCTT TTATCTGTCC TTTCCCTCAC 120
CTTCAACGGA GCACTGCTAA AAGAAGTGGG GGTTGCTGTG CACGTTGGCT CACACCTGTG 180
ATCCCAGCAT TTTGGGAGGG CAAGGTGGGC ACATCACTTG AGGTTAGGAG TTCGAGACCA 240
GCCTGGCCAA CATGGTGAAA CCGTTTCTAC TAAAAATACA AAAATTAGCC ACGCGTGGTG 300
GCACGTGCCT GTAATCCCAG CTACTTGGGA GGCTGAGGCA GGAGAATCGC TTGAACCCCA 360
GAGTTGGAGA TTGCAGTGAG CTGAGATCAG GCCACTGCAC TCCAGCCTGG GTGACAGAGG 420
GAGACTCCGT CTCAAAAAAA AACAAAAAAA AACAAAAAAA ACAGGCCGGG CGCGGCGGCT 480
CACGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCAGGT GGATCATGAG GTCAGGAGAT 540
CGAGACCATC CTGGCTAACA TGGTGAAACC CCATCTCTAC TAAAAATACA AAAAAATTAG 600
CCAGGTGTGG TGGTGGACAC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATG 660
ACGTGAACCC AGGAGGCGGA GCTTGCAGTG AGCCGAGATC GCGCCACCGC ACTCCAGGCT 720
AGGCGACAGA GTGAGACTCC GTCTAAAAAA AAAAAAAAGA AAGGAAAGAA AAGAAAGGGG 780
TTATGGGAAG GGACTTTGGA TTTGTTAGTG GAGATTCTTG GCCAGGGCAG AAGGACTCCT 840
ATTTGGCGAG TGATTCTGCT CACATATCTC CAGGGCTCTG TGTTAGTAAC TTGATTCTGG 900
GTACTTTGTG GGGAGTAGAG AGAGGAAGGG GCCGGGACAT CTACCTGGAA GGACTTAGTT 960
CTAGCTCTTG CCTACAGAAT AGTTGGTACT CAGCATAGGA CAGTGGGTAT GGTTCCAGAC 1020
CAGACTGACT TGGGGTGGGA GAGGAGAATT TTGGTCCTAG GAAGTAGAAG TGCAGCCAAG 1080
AGTGATAAAG CTCACTAAAG CAGCGGGTGT TTGGAGGGTA GTCCCTGGCA ACTCCCACTG 1140
CTTGAGTTCC AACCCCACTC TTCCTGTTCC 1170
|
