Tag | Content |
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EnhancerAtlas ID | HS095-06688 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:12163150-12164570 |
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) |
MYCN | MA0104.4 | chr12:12163357-12163369 | GGCCACGTGGCC | + | 7.22 | MYCN | MA0104.4 | chr12:12163357-12163369 | GGCCACGTGGCC | - | 7.22 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_19498 | chr12:12159217-12165094 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_39774 | chr12:12162828-12164867 | Jurkat | SE_49985 | chr12:12159945-12166471 | RPMI-8402 | SE_66709 | chr12:12162828-12164867 | Jurkat |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I012008 | chr12 | 12160347 | 12164912 |
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Enhancer Sequence | AAGCCCCTCA TCCCCAAAAG GCAAGAAATG GGGAACAACC GGGTGACTAA GGAAAACTGC 60 AAGTGAAAGC AGCTGTAATT TCTCTCGCTG TGGTTTGCGG TGCTCAACAC TCTTGCTTGG 120 CTGGTTGTCT TGGAGGGTTA ATGAGGTCTC TGCTGAGTGT CCTCAGCTTA GCAATGGGCA 180 GTGGGGCTCT GTTCACAGTC TCATCCCGGC CACGTGGCCT CCCGGGTTCA GACACCCTAG 240 GCTGATGCTG TGGTTCCATG TGCCTGAACA CGAGCATCCG AACTCATTTC CGGCCTGCCT 300 GTCCCCCCAT GCAACGGCTC CTGAAAAAGG GGAACCAAAT GCTGCCCATT TCACCCCCAT 360 CAATAGCTGA CAACGCCTGG GTTCCTGCTC TCCTGACATT CCCACTCATT GTCGTCAGTG 420 GAGCGAGCAG GCAGAGGGGA AGTGAGCTGC CTATCAGCCC CTGCAATCAG AAAAAGAGCC 480 GGGTGCCTTT AAGACGAAGG TGGTGGGCAG CCATCCATCT TCCCTAAACA CACACTCGCC 540 TTGTTCTTCC ATTTCTGGCT GAGTGATAAA AACGTTAAAT GTCATTTCCT GTATCAGTGG 600 TTAACCACTA GATGCTGGAT CAGAGATTTA CCAGAAGTGC TGAAGTTATG GAAAAAAAAT 660 AAATAAACCT GCTGTTTTCA ATAACCCTTT CTTGCACCCT GTGGGAACTA TGTAACCTCT 720 GGGGAGGGGG CTGCGAGGGG GTCGCTGGAT TTGACTTGGG CAACACACTT AGGACTAGAT 780 TTACCAAATG CTTTCTTATG CTTCATATAG GAAGTGAAGA GAGACAAAAT GTAACCATCC 840 TATACCTGTC CCCAAGTGCG CGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 900 TGTGTGTAGA AACGCTGGGA AAAGCAGGAG GAAAAATCAT CCACGTGCCT TCTTTGCCCA 960 CCTCTCTCAG GATATCTTGC AGTCATTTTG GTTTTATTGA CCCAGGGTTT TTGCAGAGGA 1020 CAGTTGCCCT GACTATTCGA TTCCCTCAGC TTCCTGCAAC AATCAATGTC CTCCAGTGAC 1080 AAGAAGGCTT CCTGGGGGAA AACATGCTCC CAGGAAACTC CTGAGAGGTG GAGAGCCCAG 1140 CTCAATCCTT TGTTGTGTCC TCTTCTTCTT TCAGTTGCTC CATTAAATTA ATCAAGAGCT 1200 CAGAAAAGGG AAGGCCTGGC TTAGCCCCCA AGGAGAGGTG ACTGGACCGA CTGCAGCCTG 1260 CCCACAGCTG TACTCCAAGC CCAGCCATGC GCTTCTGACC TGAGGTCAAC TCCCCACATA 1320 CAGCTGCCCT GGGCTCCTCC CTGCGGCCTC CCAGGCACTC CCCTCAGTCT GGACATATAA 1380 GACTTAGGAG CTGCACTTTG TTCTAGCAAT TCCATTTCCT 1420
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