| Tag | Content |
|---|
EnhancerAtlas ID | HS099-04164 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr11:63853660-63854810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYCN | MA0104.4 | chr11:63854478-63854490 | AGCCACGTGGCC | + | 6.37 | | MYCN | MA0104.4 | chr11:63854478-63854490 | AGCCACGTGGCC | - | 6.37 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_03923 | chr11:63854008-63861535 | Brain_Anterior_Caudate | | SE_04858 | chr11:63853505-63870357 | Brain_Cingulate_Gyrus | | SE_05816 | chr11:63848839-63874636 | Brain_Hippocampus_Middle | | SE_06876 | chr11:63853550-63855811 | Brain_Hippocampus_Middle_150 | | SE_07839 | chr11:63853510-63858284 | Brain_Inferior_Temporal_Lobe | | SE_65709 | chr11:63852050-63854636 | Pancreatic_islets | | SE_68066 | chr11:63823790-63896346 | TC32 |
|
| | 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 |
| GH11I064086 | chr11 | 63853927 | 63854350 |
|
Enhancer Sequence | GGCTGGAGTG GGGAGGAGGG GCTTAGCTCA GAGCCCACCC TGCCCCAGGT CTTGCATTCG 60
GGGCCAGAGG GAGGCTTCCT TTGTTGAATT GTGGTTTTAG GAGGCGTAAA GTGCATACCG 120
GCACCTGCAC AGCCTGGGGT GTGCAGTTCT AAGACCTGTG AATCTTACAT ATGCATATGG 180
TGCCCTTGTG ACTACCCCCG AGCTCAGAGG ATGGAACATT CCCTCCCCAC CCCCAGCTTT 240
CTACTCTCCA GTCCAAACCT GTCCCTCTGC TCTCCCCATG CCCTCAGGAG GAAGTCCAGG 300
CCCTTCCCTG AGGTCCCCTA GCTGACCGCC CTGCCCCAGG CTGAGTTGTC TCAGGACAGC 360
CACAAAGCCA GCCTTCCTCC TGCCTCCGGG CCTTTGCACA GCGGTTCTGC GACTGGGGTG 420
CTTTTTCCGG CCCCTGCAGC CCCACTTCTG TCTGAGACTC CTATTCATGC TCCAGGGACT 480
CACATCATGT GTTCAGGGAA GACAGAGAGG GGGAGAAGGG CATGAAGAAG GAAGGTTCTC 540
GTGCTCACAG TACAGAGATG TAGACACACC CAGATCACCC AAGCAGCTGT GGAGCTGGAC 600
GTGAGCCCTC ATCCGCTCCT CCAACTAGCC CGTGACTTCC ACAGGCGGTG CTAGGGGTGG 660
CGGCTGGGGA TGGAGCTGGG AGGGGAGGTA GCAGGCAGCC CGCTAGCCCT TCCCTGTCCT 720
GGCAGGAGCT GTCACTGCCT CTCTCCTTGA TGGCGGGGTA TGAAGAGAAG CCTTTTGACG 780
CAGGGAGATG ACCCCTCCCC GGCCTCCACC TACACAGCAG CCACGTGGCC ACCCTGAACA 840
GCTGCCACAG TGACCGACAC CCCCTGGATG TGTTTGTCCT CCCACAGCAA AGCACAATTA 900
ACATCCCCAC TGGTAAATGA TATGGGGCCA TATTTCACCT GGACCCAAAT GTGGGCCACA 960
GAGGCATTAA AATAAATGAC GGCACGGTTC AGTGAGGTCT CCGATTCTTG GATCTGGCAG 1020
AAGTGCACCT GTGCAGCGCC CCCACTGCTC TCCTGGGCCC CTGCCCCAGT TCCATGCCCT 1080
CTGTGCAGGG AAATCAACCT GCTCCTGTCA CTTCGGATGT GGGAACAGGG TCCGCCACCC 1140
AGACCTCACC 1150
|
