Tag | Content |
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EnhancerAtlas ID | HS176-08750 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:12163220-12164700 |
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 |
|
Enhancer Sequence | AGCTGTAATT TCTCTCGCTG TGGTTTGCGG TGCTCAACAC TCTTGCTTGG CTGGTTGTCT 60 TGGAGGGTTA ATGAGGTCTC TGCTGAGTGT CCTCAGCTTA GCAATGGGCA GTGGGGCTCT 120 GTTCACAGTC TCATCCCGGC CACGTGGCCT CCCGGGTTCA GACACCCTAG GCTGATGCTG 180 TGGTTCCATG TGCCTGAACA CGAGCATCCG AACTCATTTC CGGCCTGCCT GTCCCCCCAT 240 GCAACGGCTC CTGAAAAAGG GGAACCAAAT GCTGCCCATT TCACCCCCAT CAATAGCTGA 300 CAACGCCTGG GTTCCTGCTC TCCTGACATT CCCACTCATT GTCGTCAGTG GAGCGAGCAG 360 GCAGAGGGGA AGTGAGCTGC CTATCAGCCC CTGCAATCAG AAAAAGAGCC GGGTGCCTTT 420 AAGACGAAGG TGGTGGGCAG CCATCCATCT TCCCTAAACA CACACTCGCC TTGTTCTTCC 480 ATTTCTGGCT GAGTGATAAA AACGTTAAAT GTCATTTCCT GTATCAGTGG TTAACCACTA 540 GATGCTGGAT CAGAGATTTA CCAGAAGTGC TGAAGTTATG GAAAAAAAAT AAATAAACCT 600 GCTGTTTTCA ATAACCCTTT CTTGCACCCT GTGGGAACTA TGTAACCTCT GGGGAGGGGG 660 CTGCGAGGGG GTCGCTGGAT TTGACTTGGG CAACACACTT AGGACTAGAT TTACCAAATG 720 CTTTCTTATG CTTCATATAG GAAGTGAAGA GAGACAAAAT GTAACCATCC TATACCTGTC 780 CCCAAGTGCG CGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTAGA 840 AACGCTGGGA AAAGCAGGAG GAAAAATCAT CCACGTGCCT TCTTTGCCCA CCTCTCTCAG 900 GATATCTTGC AGTCATTTTG GTTTTATTGA CCCAGGGTTT TTGCAGAGGA CAGTTGCCCT 960 GACTATTCGA TTCCCTCAGC TTCCTGCAAC AATCAATGTC CTCCAGTGAC AAGAAGGCTT 1020 CCTGGGGGAA AACATGCTCC CAGGAAACTC CTGAGAGGTG GAGAGCCCAG CTCAATCCTT 1080 TGTTGTGTCC TCTTCTTCTT TCAGTTGCTC CATTAAATTA ATCAAGAGCT CAGAAAAGGG 1140 AAGGCCTGGC TTAGCCCCCA AGGAGAGGTG ACTGGACCGA CTGCAGCCTG CCCACAGCTG 1200 TACTCCAAGC CCAGCCATGC GCTTCTGACC TGAGGTCAAC TCCCCACATA CAGCTGCCCT 1260 GGGCTCCTCC CTGCGGCCTC CCAGGCACTC CCCTCAGTCT GGACATATAA GACTTAGGAG 1320 CTGCACTTTG TTCTAGCAAT TCCATTTCCT TCCCAGTGCC AGTTGGGATG TGCTGTGCAC 1380 ACCAAGTGCC CCTAGCTCCT CACCTACCTC TGGGATCACT GACAGTCCTG CTTTACCTGG 1440 GACCGAAGGG ATTCATGGGG CGGCCGGGGC GGGGGAGGGA 1480
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