| Tag | Content |
|---|
EnhancerAtlas ID | HS039-03112 |
Organism | Homo sapiens |
Tissue/cell | ESC_NPC |
Coordinate | chr16:80971590-80972860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr16:80972589-80972599 | TTTAATTAGA | - | 6.02 | | RARA(var.2) | MA0730.1 | chr16:80971601-80971618 | AGGTCAAACAGAGGTGA | + | 6.48 | | TEAD1 | MA0090.2 | chr16:80972088-80972098 | CACATTCCAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_35058 | chr16:80964500-80974093 | HeLa | | SE_38132 | chr16:80964874-80974069 | HUVEC |
|
| | 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 |
| GH16I080935 | chr16 | 80969476 | 80973948 |
|
Enhancer Sequence | GAAATTGCCC AAGGTCAAAC AGAGGTGAGT GGCAGAGAAC TCAGGAGGTA GGGCTCCAAC 60
TCAGCCTCCA TCAACATGAG AAAATGCACG TCAATATTTG GATCCTGTCA GTGAAAGCAG 120
GGTGAAGTTA TGCCTCAGTT TAAGGAGGGA GCTGGAAGCA GTTTTGATGC CTCCACTGAG 180
GCATGTTTGC CCCAGGAGAT GTAGGGTCTC CTCCTGGCTT ACGTAAAGAA CCAGTGTGTT 240
AGTCAGTATT CTGTTGTAAC CCAGACTCCA AAACTCTCCG TGGTTTACAG CAGAGGTTTA 300
ATTCTTGCAC TCAAGTCTGC AGCTCAGCTG CCTCTGCTTA GCTCTGCTCC CATCTTCTCA 360
CTCCAGGACT CAGGCTGAAA GAGCAGCATC ATCTGGGAAC TGTGGAGCTT ACAGCAGAAA 420
GCAGTAAGGC AAGAGGCCAA GCCAAACTAT GCAATCTCAT TGAAAGCTTC TGCTCAGACA 480
GCATAAATCA TGTCCGCTCA CATTCCATTG GAAGAAGCGA GTCACAAGGC CAAACCTGCC 540
AACATACTCC CCTTACTGGA TTGCTCCTGG AAGTCACGTG GCAAACGGTG TTGGACGTGT 600
AATACCCTCA GACAGAGGCA GAAGATAGTT GCAAACAATA ACATAATCGG TCGTACCAAG 660
AAACAAGTGC TGGAACAATG GGACTTAAGG ATAAATCTGC CTTTCACAGC AGGGAGCCCC 720
CCAGTGGGGC GAATGGAAGA GAATATAAAG TTCCCAGGCT CTTGAATTGA ACAAAGACGG 780
AGTCTCAGCT GCAGACAGGC CAAATTCCAG TGGCAAAAAC AATGTCCTGA GAGCCAGAGC 840
TTCCAACATC TGGAGCCCAA ACAGGGACCT AACAAAAGAT CAGAATACAA TGACCCCGGG 900
GGATGCCTGA CGAGTGTATC GTAAGAATAA TCATTGTCTC TGGGCATTGG GTTATGAGTA 960
ATATCCTCTT CTGTTTTCTA CTGAGTGATT GTGCTACTTT TTAATTAGAA AAAGAAGCAT 1020
TTTAGAAAAG TATATGTGTC CTCCCTGGAG CCGAAAACAG CATGGGGCAG CAGAAGTGAC 1080
TGCTTTTCCA TGCCAAACCT CACACTGATG AGAAAGATTT GCATGTCCGA TGACGCACCA 1140
AAGGTGTGTA ATTTCAATCC CCTGGGGCAA ATGGTCCTGC CATCTACTGT AACGACTGAT 1200
AAATGGGAAG GCAATAATAA GCATAATCTT TTTTTCTCAG GTGTTTTCTT TTTGGCAGGG 1260
GTGGATGGGG 1270
|
