| Tag | Content |
|---|
EnhancerAtlas ID | HS176-40428 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr8:103733490-103734830 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr8:103734232-103734243 | TTCAAGGTCAT | + | 6.62 | | Esrrg | MA0643.1 | chr8:103734233-103734243 | TCAAGGTCAT | + | 6.02 | | Myog | MA0500.1 | chr8:103734092-103734103 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr8:103734092-103734103 | CTGCAGCTGTC | - | 6.14 | | ZNF263 | MA0528.1 | chr8:103734555-103734576 | CCCTTTCCTCCTTCCTCCATC | - | 6.52 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33791 | chr8:103733042-103735520 | HCC1954 | | SE_37665 | chr8:103733343-103734961 | HSMMtube |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I102720 | chr8 | 103733100 | 103734770 |
|
Enhancer Sequence | TTAAAAAAAT AAGATTAAAA AAATTTTTTT TAACGAAGAC GGGGCCACCT TAACGGCTAC 60
TGTAAGAGTT ACCAATCAGC TTGAGGAGCT GGAGAGAATG GATTTTGGGG TGGGGACACT 120
CAAGGAGCAG AAAAGTGCTC CGAAGGGCAG GGCTTCCTCA CTGTGCTTGA GACTGCTCTC 180
TGGACTTCAG GGAGTTGTGA ACCTCCTACA AGTGTGTGGA AATCATGCAT ACGTAGGTAT 240
GTGCATTTTT CAGGGGTAAG TAGTCTCACT GAGGTAAACG AGGAAGACCA GGCATTGTTG 300
ACCAAGTTCT GTCCCGGCCT GGGTGGAACT ATTTGTAAGA TGATGCCACC TCCATGACCA 360
GAAACTGACC TTCTTGGGAT GATTTTTTCC CAACATTTCT TAAATTTCCA ACTTTATTTC 420
TTCAAAGCTC TTCTCCATCT AGTTGGGCTG TACTTTCTGG CTCTCCAGGA ACTTTCAGCT 480
GTCAGTATTC CCTGCTTAAT GCCTGTCAAT TTCTCTATAC AGTAGCTTCC TGCCTGTCAG 540
GTCTGGACAT GCTCAAAAAT CCCTTCCACA TTGGGTGGCG TCTGGGAAGT GGCTTTCTTT 600
CCCTGCAGCT GTCCATTTGC CTCTTTTCTC CCAGCCTGGC TTCTGAAAAG ATTTATGAAC 660
ATTTGTTATC TCTGCTTATC TCTTAGTCAG ACTTCAGCTT GATCCAATCT GTTTTCCACC 720
TTTTTCTACC GAAACTTCTC TCTTCAAGGT CATCGGTTTG CCAAATCTAA TTCTAATGGA 780
CCAGTTTCCA TTCTTACCTT GCTTGTTTTC TCAGTGGGAT TTTATGCTTA TATTTCCTCC 840
TCCCTGAAGC TTTCCCCTCC TTGACCCTCT AAGTAGGGAA TATATGATTA ATCTCCCAAA 900
CTGGGTCACT GTTTAAAGTG AAAGGGGGCA CTAATGAATA ATTATGCCAG GCTCACTGTC 960
ATAAGCCAAG ACTCCCAGGC ACACTCAGAC GTGTGGTCAC CCTCCCTGCA AAACTTGCTT 1020
TCCCTTCCCT GGGCTGCTCA GCCTTCTCAT ACTCCTTCAT GGGATCCCTT TCCTCCTTCC 1080
TCCATCCACT GTCCACTCCT TAAAACTGCC CTGGGCTCTC CCCTGCTCTC ATGCTACACC 1140
ATCTCCCTGA GTGATCTTTT TTTTTGAGAC GGAGTTTTGC TCTTGTTGCC CAGGCTGGAG 1200
TGCAATGGCA TGATCTCAGC TCACCACGAC CTCCGCCTCC CAGGTTCAAG CAATTCTCCT 1260
GTCTCAGCCT CCCGAGTAGC TGGGATTACA GGCATGCGCC ACCACGCCCG GCTAATTCTG 1320
TATTTTTAGT AGAGATGGGG 1340
|
