| Tag | Content |
|---|
EnhancerAtlas ID | HS095-29871 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr8:103733450-103734720 |
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 | TCTTTTAAAA TGAAGAAGGG TCTTTTTGGT AGGAGATGGC TTAAAAAAAT AAGATTAAAA 60
AAATTTTTTT TAACGAAGAC GGGGCCACCT TAACGGCTAC TGTAAGAGTT ACCAATCAGC 120
TTGAGGAGCT GGAGAGAATG GATTTTGGGG TGGGGACACT CAAGGAGCAG AAAAGTGCTC 180
CGAAGGGCAG GGCTTCCTCA CTGTGCTTGA GACTGCTCTC TGGACTTCAG GGAGTTGTGA 240
ACCTCCTACA AGTGTGTGGA AATCATGCAT ACGTAGGTAT GTGCATTTTT CAGGGGTAAG 300
TAGTCTCACT GAGGTAAACG AGGAAGACCA GGCATTGTTG ACCAAGTTCT GTCCCGGCCT 360
GGGTGGAACT ATTTGTAAGA TGATGCCACC TCCATGACCA GAAACTGACC TTCTTGGGAT 420
GATTTTTTCC CAACATTTCT TAAATTTCCA ACTTTATTTC TTCAAAGCTC TTCTCCATCT 480
AGTTGGGCTG TACTTTCTGG CTCTCCAGGA ACTTTCAGCT GTCAGTATTC CCTGCTTAAT 540
GCCTGTCAAT TTCTCTATAC AGTAGCTTCC TGCCTGTCAG GTCTGGACAT GCTCAAAAAT 600
CCCTTCCACA TTGGGTGGCG TCTGGGAAGT GGCTTTCTTT CCCTGCAGCT GTCCATTTGC 660
CTCTTTTCTC CCAGCCTGGC TTCTGAAAAG ATTTATGAAC ATTTGTTATC TCTGCTTATC 720
TCTTAGTCAG ACTTCAGCTT GATCCAATCT GTTTTCCACC TTTTTCTACC GAAACTTCTC 780
TCTTCAAGGT CATCGGTTTG CCAAATCTAA TTCTAATGGA CCAGTTTCCA TTCTTACCTT 840
GCTTGTTTTC TCAGTGGGAT TTTATGCTTA TATTTCCTCC TCCCTGAAGC TTTCCCCTCC 900
TTGACCCTCT AAGTAGGGAA TATATGATTA ATCTCCCAAA CTGGGTCACT GTTTAAAGTG 960
AAAGGGGGCA CTAATGAATA ATTATGCCAG GCTCACTGTC ATAAGCCAAG ACTCCCAGGC 1020
ACACTCAGAC GTGTGGTCAC CCTCCCTGCA AAACTTGCTT TCCCTTCCCT GGGCTGCTCA 1080
GCCTTCTCAT ACTCCTTCAT GGGATCCCTT TCCTCCTTCC TCCATCCACT GTCCACTCCT 1140
TAAAACTGCC CTGGGCTCTC CCCTGCTCTC ATGCTACACC ATCTCCCTGA GTGATCTTTT 1200
TTTTTGAGAC GGAGTTTTGC TCTTGTTGCC CAGGCTGGAG TGCAATGGCA TGATCTCAGC 1260
TCACCACGAC 1270
|
