| Tag | Content |
|---|
EnhancerAtlas ID | HS098-11294 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:112434980-112436000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr11:112435911-112435927 | GATTCCTCGAGAGCAC | - | 6.91 | | FOSL1 | MA0477.1 | chr11:112435219-112435230 | AGTGACTCATG | + | 6.14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I112563 | chr11 | 112434580 | 112435878 |
|
Enhancer Sequence | TATATAGACA GGGCTTAAAA GTGGCTGCTA AAATGGGACT GGACCGGTGC CTGTGAGCTC 60
AAACACAAGT TCACATACTC TCCTCAAGCA GGCCTAGCAT CCACCCCCCT CCCTAGGGTT 120
CCAGTTTGGT TCTAAGTAGT TTTTGGCTCA CAGCATCTTT TGTTGTTCTC TGCACTGCAG 180
AGATATTTGC TGTCACTTTG TTGTCAGACC CAGGAAACGT TGTCTGGCTC CCAGAGGTCA 240
GTGACTCATG GACTCACGGT AGACACACAG ATTGTTTGTG AGCTAGGGCT TGCTGGAGAG 300
TATCTGGATA AACAAGAGAA ACCCAAATCA GGCTGTCTCT CTGCCTGCTG AGAGCACTGT 360
TTATTGTTCC AGCCTCAGTG TTTGGAAATG TAAACCTCTG GCTGACTTTT CACTCCTCTG 420
GCTTCACCAC AGAGTTCAGA AATCCACTGT GGCCACAAAG GCTGTTTTGG AAGAGCTTTC 480
TCTCTTTAGC TGTCTCTGCA GTTTTAGGAT GCTGGAAGCC ATTTGCTTTT CTGATTTAAG 540
AACATTTTTC CTGGAGTGAG GGAGGGAAAG TCCAGGGTCT GATTGGTGAG GCTGCAGGGG 600
TGGAACTGGG TCACCTGGAC CTGGGATGCC TGCAACTTGT GGGCTGGCTG GTTAAACCAT 660
GAGAGGGGAC AGGCCCCCCT CTCTCAGGTA TGGTCCTGGC CTTTAGTCCT GGTCTTTCCC 720
ACAACTAGGG CCCTTACCTG ATTGTTGGTG CCAGCTCAGA CCCTGGGAGT CTGGTATTAT 780
GGTTTCTCAT TTCCAGAAAT GTTTCTTTGG GGTCATTGGT GTCAGGTATG GGGAGATAAA 840
GTATGGCTCC TTTTCTTAGG AATTCATAGT CTAGTTGGAA AGAGAGAGAA AATAATGAGT 900
AGTGGTCAAT GCCCTAACAA GGCTAGGAGA AGATTCCTCG AGAGCACAAA GGGGACAGAG 960
TAACTTAGCT TGTCTGGGGA GGTGGGTGAC TTGGACCAAA TCCTAAAGTA GGAGCAGGAA 1020
|
