| Tag | Content |
|---|
EnhancerAtlas ID | HS170-00755 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr12:12162850-12164580 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| | 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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I012008 | chr12 | 12160347 | 12164912 |
|
Enhancer Sequence | CAGAGTGCTG GGATTACAGG TGTGAGCTAC CGCACCCAGC CAAGAGATTG TTTAATCAGC 60
AAAAGGCTGG GCAGGGCAGT GGGGCCTAGG GCGGCACTTG CTATCAGATG TCTGGAGGGC 120
AGGGTTGGCT TTGGCCATAG ATGGACCTCG GTTCAAATCC TGGCTGGCCA TACCACTTAC 180
CAGCTCTAGA CCTAGAGCAG GTTAACATCA TGAATCTAAA CTACTTACCA CTTAACAAAG 240
TGAGTGACTA TCTATAACTG TTGCCGTTGT TACAAGAAAT CCACTTAGTA ACTGCACTGA 300
AAGCCCCTCA TCCCCAAAAG GCAAGAAATG GGGAACAACC GGGTGACTAA GGAAAACTGC 360
AAGTGAAAGC AGCTGTAATT TCTCTCGCTG TGGTTTGCGG TGCTCAACAC TCTTGCTTGG 420
CTGGTTGTCT TGGAGGGTTA ATGAGGTCTC TGCTGAGTGT CCTCAGCTTA GCAATGGGCA 480
GTGGGGCTCT GTTCACAGTC TCATCCCGGC CACGTGGCCT CCCGGGTTCA GACACCCTAG 540
GCTGATGCTG TGGTTCCATG TGCCTGAACA CGAGCATCCG AACTCATTTC CGGCCTGCCT 600
GTCCCCCCAT GCAACGGCTC CTGAAAAAGG GGAACCAAAT GCTGCCCATT TCACCCCCAT 660
CAATAGCTGA CAACGCCTGG GTTCCTGCTC TCCTGACATT CCCACTCATT GTCGTCAGTG 720
GAGCGAGCAG GCAGAGGGGA AGTGAGCTGC CTATCAGCCC CTGCAATCAG AAAAAGAGCC 780
GGGTGCCTTT AAGACGAAGG TGGTGGGCAG CCATCCATCT TCCCTAAACA CACACTCGCC 840
TTGTTCTTCC ATTTCTGGCT GAGTGATAAA AACGTTAAAT GTCATTTCCT GTATCAGTGG 900
TTAACCACTA GATGCTGGAT CAGAGATTTA CCAGAAGTGC TGAAGTTATG GAAAAAAAAT 960
AAATAAACCT GCTGTTTTCA ATAACCCTTT CTTGCACCCT GTGGGAACTA TGTAACCTCT 1020
GGGGAGGGGG CTGCGAGGGG GTCGCTGGAT TTGACTTGGG CAACACACTT AGGACTAGAT 1080
TTACCAAATG CTTTCTTATG CTTCATATAG GAAGTGAAGA GAGACAAAAT GTAACCATCC 1140
TATACCTGTC CCCAAGTGCG CGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 1200
TGTGTGTAGA AACGCTGGGA AAAGCAGGAG GAAAAATCAT CCACGTGCCT TCTTTGCCCA 1260
CCTCTCTCAG GATATCTTGC AGTCATTTTG GTTTTATTGA CCCAGGGTTT TTGCAGAGGA 1320
CAGTTGCCCT GACTATTCGA TTCCCTCAGC TTCCTGCAAC AATCAATGTC CTCCAGTGAC 1380
AAGAAGGCTT CCTGGGGGAA AACATGCTCC CAGGAAACTC CTGAGAGGTG GAGAGCCCAG 1440
CTCAATCCTT TGTTGTGTCC TCTTCTTCTT TCAGTTGCTC CATTAAATTA ATCAAGAGCT 1500
CAGAAAAGGG AAGGCCTGGC TTAGCCCCCA AGGAGAGGTG ACTGGACCGA CTGCAGCCTG 1560
CCCACAGCTG TACTCCAAGC CCAGCCATGC GCTTCTGACC TGAGGTCAAC TCCCCACATA 1620
CAGCTGCCCT GGGCTCCTCC CTGCGGCCTC CCAGGCACTC CCCTCAGTCT GGACATATAA 1680
GACTTAGGAG CTGCACTTTG TTCTAGCAAT TCCATTTCCT TCCCAGTGCC 1730
|
