| Tag | Content |
|---|
EnhancerAtlas ID | HS062-04222 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:115100080-115101040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:115100576-115100595 | GCACCAGCAGATGGCGGCA | + | 6.4 | | STAT1 | MA0137.3 | chr12:115100411-115100422 | TTTCCAGGAAA | + | 6.62 | | Stat4 | MA0518.1 | chr12:115100411-115100425 | TTTCCAGGAAATGG | + | 8.42 | | ZNF263 | MA0528.1 | chr12:115100690-115100711 | TTTCCCCCATCCTCCACCTTC | - | 6.08 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I114662 | chr12 | 115099697 | 115101283 |
|
Enhancer Sequence | AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAACCTC TGTCTTTGTT 60
GGAATTTCCA AAACGGGAAG GAAGTAGGAA CTATTGACAG AGCAGGTGCT TTGCAAGGAT 120
ATTTGTCCCT TGCTCTTTAC AGCACATCTG CCTGTAAGGA TGTGGGTATC ATTATTCCAC 180
TTTTATTTTA TGAGGAATTA AGACCCAGAA AAGTTAAGCC ACCTGGCCAA AGGACACTCA 240
AAAAGTAGGT GGCAAAGCCA GGACTCCAGT CCCATTTTTC TGCCTCCAAA TTCTAGTTAT 300
TTGCCTTGCC ACCATTCTCT CTATCTCTTA GTTTCCAGGA AATGGCCATG GGGTTTGCTT 360
CACTGGAATG CAATTCCATG AGAACAGAGA CCATGTCCCA GTGATGATTA ATTGCTGAAT 420
AAATGAATGA TAACGTAAAT GAGTATGTGA CTCAGCCTTC CAGAAGTATT GGAAAAGCCC 480
CATGCACTTT CCTATGGCAC CAGCAGATGG CGGCAAAAGA GCAGCTTAGC AAAGGCAGAG 540
GCAAACACTT GGCGTTTCTT TCATTTATGT ATCCTCTCTT CCTTGATCTT TGCAAAACAG 600
GTAGCTTGCA TTTCCCCCAT CCTCCACCTT CACTACTCCC CTCCCCCCAT TCTGGGAGGA 660
ACCAAGAGGT AGTGCTCACA GACTGCAGTC CCCTCTTTCT GTTTTGACCT CTTTGCCCCA 720
CCTCAGAGAC AAGGTTATTT CAAGAAATGG AAGAAGAAAT AACACCAGAA GAACTTTAAT 780
GGCAATGAAA ACCAGTGCAG AAATGACCTT TTTATTGACA AATAGAGAAA AGGTATCATG 840
TCCCCAGCTG CTGATGAGGC AGACACAGAC TGTCCCCCAA CATTGGCCTC ATCATCCATA 900
CTTTTGTGAT TTGCCTTGAA GGGAAGTATG GGGTAGAATA GAGGTGGGCA GGGGGAATTT 960
|
