Tag | Content |
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EnhancerAtlas ID | HS019-06189 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr16:30092630-30093800 |
Target genes | Number: 44 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr16:30092929-30092939 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr16:30092929-30092939 | GGCACGTGCC | - | 6.02 | IRF1 | MA0050.2 | chr16:30093377-30093398 | AAAAAAAAAAAGAAAGGAAAG | - | 6.2 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_31719 | chr16:30092037-30092861 | Gastric | SE_35600 | chr16:30091964-30093106 | HepG2 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I030080 | chr16 | 30091965 | 30093106 |
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Enhancer Sequence | AGTGAGTACC TGCTGTCCCT GCAGAGCCAG GCCTGGTCTT TCAGGCACAT GAAGTTTCCT 60 CTTCATCTTG GGGGCTCTAT AAGCCCAACC CTAAGCTCTT TTATCTGTCC TTTCCCTCAC 120 CTTCAACGGA GCACTGCTAA AAGAAGTGGG GGTTGCTGTG CACGTTGGCT CACACCTGTG 180 ATCCCAGCAT TTTGGGAGGG CAAGGTGGGC ACATCACTTG AGGTTAGGAG TTCGAGACCA 240 GCCTGGCCAA CATGGTGAAA CCGTTTCTAC TAAAAATACA AAAATTAGCC ACGCGTGGTG 300 GCACGTGCCT GTAATCCCAG CTACTTGGGA GGCTGAGGCA GGAGAATCGC TTGAACCCCA 360 GAGTTGGAGA TTGCAGTGAG CTGAGATCAG GCCACTGCAC TCCAGCCTGG GTGACAGAGG 420 GAGACTCCGT CTCAAAAAAA AACAAAAAAA AACAAAAAAA ACAGGCCGGG CGCGGCGGCT 480 CACGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCAGGT GGATCATGAG GTCAGGAGAT 540 CGAGACCATC CTGGCTAACA TGGTGAAACC CCATCTCTAC TAAAAATACA AAAAAATTAG 600 CCAGGTGTGG TGGTGGACAC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATG 660 ACGTGAACCC AGGAGGCGGA GCTTGCAGTG AGCCGAGATC GCGCCACCGC ACTCCAGGCT 720 AGGCGACAGA GTGAGACTCC GTCTAAAAAA AAAAAAAAGA AAGGAAAGAA AAGAAAGGGG 780 TTATGGGAAG GGACTTTGGA TTTGTTAGTG GAGATTCTTG GCCAGGGCAG AAGGACTCCT 840 ATTTGGCGAG TGATTCTGCT CACATATCTC CAGGGCTCTG TGTTAGTAAC TTGATTCTGG 900 GTACTTTGTG GGGAGTAGAG AGAGGAAGGG GCCGGGACAT CTACCTGGAA GGACTTAGTT 960 CTAGCTCTTG CCTACAGAAT AGTTGGTACT CAGCATAGGA CAGTGGGTAT GGTTCCAGAC 1020 CAGACTGACT TGGGGTGGGA GAGGAGAATT TTGGTCCTAG GAAGTAGAAG TGCAGCCAAG 1080 AGTGATAAAG CTCACTAAAG CAGCGGGTGT TTGGAGGGTA GTCCCTGGCA ACTCCCACTG 1140 CTTGAGTTCC AACCCCACTC TTCCTGTTCC 1170
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