| Tag | Content |
|---|
EnhancerAtlas ID | HS150-06019 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr2:113449730-113450930 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr2:113450812-113450823 | GATGAGTCACT | - | 6.02 | | JUND | MA0491.1 | chr2:113450812-113450823 | GATGAGTCACT | - | 6.32 | | Nfe2l2 | MA0150.2 | chr2:113450253-113450268 | TGCTGACTCATGCTG | - | 7.41 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_10045 | chr2:113447710-113451690 | CD14 | | SE_40073 | chr2:113448416-113451173 | K562 |
|
| | 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 |
| GH02I112690 | chr2 | 113448115 | 113451494 |
|
Enhancer Sequence | TGTAGAACCT GGGAGTGAGG CTTGGCAGGA AATCTGCAGT GAGAAATGTC ACAACCCAAA 60
CAGTAACTCA TACACAGAGC TTCGCATGTC TCATTCCACA AGGATCAGCA GCTGGACCAT 120
TACCTGGAGC TATAGACTTG ATGAAAGCCC CAGAAATGGC TAAGGCAGAG GAAGTGCCTG 180
GGAGTTGTTT GGCAATTTGA CACAATATCT TTTAGATATT TTTAAAGCCA CTGAGCAAAT 240
CAAATCCTCA AGTTTAGGGA TGGATTCAAA GGCCAGTCCT TTCACTATCG GACTGGAATG 300
ATTTTTAGTC ATCTTACCTC TCAGCATTTA CTCCTTTTCC CAGATGCAGC AGCCCCACCT 360
CCTTCCAGGG AGTCACCTGT CCAGGTCAGG TGCCTCCTCA GGGGAAGCAT CCCTCACCCG 420
CCAGATTGCC AGGGCGTGTG ACTCTATCTG GGCCAACCAC ATCCTCTCTC CTGGACTTTG 480
ACTGCTGCGA GGAGTGAGGC TAGAACCAGA GAAACCTAGC TGATGCTGAC TCATGCTGGA 540
GGTTCCTGCG GAGTGAGCAT CAGAGCTCAT GAGCTCATCT CCCTAGAAAC CAGCATGCCT 600
GAACTTGACC TCTGGCTTCT GCAGCCAGGC GGCAACTGTA ACAACAGCAA CTCCCTCCCT 660
ACTCCTCAGG GCCCATATCT GCCCAGCTTC TCCTGCCTTG GTCCAGTGTG GTCTGTACTC 720
CTCCTGTGCT GTCCTCCCAG CCCCTCCACC ATTCTGGCTT CCTGTTAGGT AGAGACCCCC 780
TTGACCCATC CCATACCTCC CTCACTTCCA TGCCCACCTG GGAGCTGCAA CCAGAGCCAG 840
CTAAAGCTCT GCATCCCCCA ACCCAAGTAC ACCTTCATTG TCCCTCCAAA GCCCTGTCTC 900
ACCTCAATGA GATGCCTCAC TGAGATGCTG GAACCATTTC ATCCTCAGTA ATTGGGGTCA 960
GTTTCTCCCC AGTCCTGTGA CTTCTGCCTC TTGTCACCCT GAGGGCAGGC AGGAGAGCCC 1020
TGGTGTGGCA AAGCTGGTTG GGGAGCAAAT GGGCACAGGA GAGAAGAGGG AAGGTGTGGG 1080
AGGATGAGTC ACTGGCAGAG TGGGCAGGGG CGCTAAGGAA GGGAATGAGT GCATGGACCT 1140
GGGCTTGATG GTTCAGCTAC TGAACACCAA GATGCTGCAA TTTGAGAGTT CCAGAAAGTT 1200
|
