| Tag | Content |
|---|
EnhancerAtlas ID | HS098-21908 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:56984930-56986170 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr16:56985743-56985764 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | | IRF1 | MA0050.2 | chr16:56985749-56985770 | TTTTTCTTTTTCTTTCTTTTC | + | 6.31 | | NFAT5 | MA0606.1 | chr16:56986126-56986136 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr16:56986126-56986136 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr16:56986126-56986136 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_10250 | chr16:56984613-56985906 | CD19_Primary | | SE_54184 | chr16:56984512-56985592 | Spleen | | SE_60786 | chr16:56944371-56985827 | DHL6 | | SE_61229 | chr16:56943702-57048981 | HBL1 | | SE_61952 | chr16:56944457-57039420 | Toledo | | SE_62533 | chr16:56944126-56985732 | Tonsil |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I056950 | chr16 | 56984775 | 56986092 |
|
Enhancer Sequence | TGTGTGTCCT GCACGGTGGC AGGTGTCTGA AGCTGAGCCC AGAGGAGCTG TGGAGATCAG 60
GCCCAGAAGT GGAGCCACAG CACGTAGGGC CAGAGACCTG CAGTAAGAAA TGGGATGTGG 120
TCGAGATGGG ATGGGAGCCA CCGCAGCACC ATGGGGCGGG AGCAGCAGAG TCTGATGTTG 180
TGTACTTCAG GGAGCTGGAG TTCTATGAAG GAAGAGCGAG GAGGCATGTG GGAGGAAGAA 240
CAGCCCCACT GAGGCCTGCA GGGAAGGCAG CAGACCCCAG GTCAGAGCAT GAAGGTAGAG 300
GGGAGGTTCC AAGAAGTGGG TTGGGGAATA AGCACTGGAT GGCTGATGAC AGAGGGCAGG 360
GTGGAGGATG CGGGGCCAGG GAGGGCTGCA CAGAGTCCTG GGAGGGTGAG CGGTGGCCCT 420
GGCTGGCTAG GAGGCGCCAC CTTGAGGTGC TACTGGAGGA TACGCCGCAG GGAAGGTGGA 480
TGGTCTCTTC TGATGACAAC CTTCTTGCTG GCATTAGACT GAAAGGGGAG GTGATTTGTA 540
GGGATGAGGC CAGAGGGGTT GTCCCCAGGG AAGGGCACCA GATGTGGGGC AGGAGAGCTG 600
GTGTGAGTTG CAGCCGTGGG GCCTAGAGGA AGTCACAGCA CCCCACTGAA TTCTCACTTC 660
CTCATCATAA CAGACCCTGT GACATATAAA ACCTGCTCTG CCCACCGCAC AGGGATCACA 720
AGGCTGGAGT GAAATAATGG AGCACTTCCC CAGAGTGGCA CACGGGACCC AGGGACGGGT 780
GTGCAAAACC GTTCTAGGTG GAAGAACACT TTTTTTTTCT TTTTCTTTTT CTTTCTTTTC 840
CTTTTTTTTT TTTTTTTTTT TGAGATGGAG TCTCCGTCTG TTGCCCAGGC TGGAGTGCAG 900
TGGTGCAATC TTGGCCCACT GTAGTCCCTG GCTCCCAGGT TCAAGTAATT CTCCTGCCTC 960
AGCCTTCTGA GTAGCTGGGA CTACAGGCAC CCACCACAAC ATCTAGCTAA TTTTTGTATT 1020
TTTAGTAGAG ACAGGGTTTT ACCATGTTGA CCAGACTGGT CTTGAACTCC TGACGTCAAG 1080
GGATCCATCT GCCTTGGCCT ACCAAAGTAG CTGGGATTAC AAGCATGAGC CACCGTGCAA 1140
AGCCAAAAAC ACTTGATTAT AATAGCATGC TATTTTTCAA TGTATTAGAT AAATGTATTT 1200
TCCATTTAAA GTGGGGATAT AAAGCTCCCC TTTAAAATCC 1240
|
