| Tag | Content |
|---|
EnhancerAtlas ID | HS098-12397 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:12163180-12164760 |
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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I012008 | chr12 | 12160347 | 12164912 |
|
Enhancer Sequence | GGGAACAACC GGGTGACTAA GGAAAACTGC AAGTGAAAGC AGCTGTAATT TCTCTCGCTG 60
TGGTTTGCGG TGCTCAACAC TCTTGCTTGG CTGGTTGTCT TGGAGGGTTA ATGAGGTCTC 120
TGCTGAGTGT CCTCAGCTTA GCAATGGGCA GTGGGGCTCT GTTCACAGTC TCATCCCGGC 180
CACGTGGCCT CCCGGGTTCA GACACCCTAG GCTGATGCTG TGGTTCCATG TGCCTGAACA 240
CGAGCATCCG AACTCATTTC CGGCCTGCCT GTCCCCCCAT GCAACGGCTC CTGAAAAAGG 300
GGAACCAAAT GCTGCCCATT TCACCCCCAT CAATAGCTGA CAACGCCTGG GTTCCTGCTC 360
TCCTGACATT CCCACTCATT GTCGTCAGTG GAGCGAGCAG GCAGAGGGGA AGTGAGCTGC 420
CTATCAGCCC CTGCAATCAG AAAAAGAGCC GGGTGCCTTT AAGACGAAGG TGGTGGGCAG 480
CCATCCATCT TCCCTAAACA CACACTCGCC TTGTTCTTCC ATTTCTGGCT GAGTGATAAA 540
AACGTTAAAT GTCATTTCCT GTATCAGTGG TTAACCACTA GATGCTGGAT CAGAGATTTA 600
CCAGAAGTGC TGAAGTTATG GAAAAAAAAT AAATAAACCT GCTGTTTTCA ATAACCCTTT 660
CTTGCACCCT GTGGGAACTA TGTAACCTCT GGGGAGGGGG CTGCGAGGGG GTCGCTGGAT 720
TTGACTTGGG CAACACACTT AGGACTAGAT TTACCAAATG CTTTCTTATG CTTCATATAG 780
GAAGTGAAGA GAGACAAAAT GTAACCATCC TATACCTGTC CCCAAGTGCG CGTGTGTGTG 840
TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTAGA AACGCTGGGA AAAGCAGGAG 900
GAAAAATCAT CCACGTGCCT TCTTTGCCCA CCTCTCTCAG GATATCTTGC AGTCATTTTG 960
GTTTTATTGA CCCAGGGTTT TTGCAGAGGA CAGTTGCCCT GACTATTCGA TTCCCTCAGC 1020
TTCCTGCAAC AATCAATGTC CTCCAGTGAC AAGAAGGCTT CCTGGGGGAA AACATGCTCC 1080
CAGGAAACTC CTGAGAGGTG GAGAGCCCAG CTCAATCCTT TGTTGTGTCC TCTTCTTCTT 1140
TCAGTTGCTC CATTAAATTA ATCAAGAGCT CAGAAAAGGG AAGGCCTGGC TTAGCCCCCA 1200
AGGAGAGGTG ACTGGACCGA CTGCAGCCTG CCCACAGCTG TACTCCAAGC CCAGCCATGC 1260
GCTTCTGACC TGAGGTCAAC TCCCCACATA CAGCTGCCCT GGGCTCCTCC CTGCGGCCTC 1320
CCAGGCACTC CCCTCAGTCT GGACATATAA GACTTAGGAG CTGCACTTTG TTCTAGCAAT 1380
TCCATTTCCT TCCCAGTGCC AGTTGGGATG TGCTGTGCAC ACCAAGTGCC CCTAGCTCCT 1440
CACCTACCTC TGGGATCACT GACAGTCCTG CTTTACCTGG GACCGAAGGG ATTCATGGGG 1500
CGGCCGGGGC GGGGGAGGGA GGACTTTTGT TTCTAAAACT GGGAAAGTCC CAGGCAAACC 1560
GAAATGAATT GGTCACCCCC 1580
|
