| Tag | Content |
|---|
EnhancerAtlas ID | HS024-06056 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr16:67896050-67898180 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr16:67897240-67897252 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr16:67897240-67897252 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr16:67897239-67897254 | TTCTATTTTTAGTGC | - | 6 | | NFIC | MA0161.2 | chr16:67897113-67897124 | TTCTTGGCAGA | + | 6.02 |
|
| | 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 |
| GH16I067860 | chr16 | 67894150 | 67898265 |
|
Enhancer Sequence | AGCATGGTCA GCTTTGTGGT TTAGAGCTCA GGGATGCAGA GTTAGCAGAA AAAAGAGACG 60
GGCCTTGACC AGAGGACCCA GTGTCAGCAC TGATGTACCA GGTGAGCTTA GGGCAAGACC 120
CAGCGACATC ACTGGATGAC AGTGGATTCT GACTATGTGG CTGTTGTGAT CACTACTTGG 180
AAATAAACAC AAGACAGTGA AGCAGGCCTC AATCCCACAT AGTTTTGAAG GTTCCTTGTC 240
ATTTTCTGGG AGCCCCTGAT GTGTCCTATT CCTCAGAGAG CTTACTCTTC CCCACTCTTC 300
TCTGCCCTAC CAGGCCAAAG GGTCTTTCTC TTCCTTTATC CCTCCACCCC ATTTCCTTCC 360
ACCACCACTT CAGTCAAGGA GTTTTTGTAT CAGAAAGTTA TCACAGGCCA GTTATGGTGG 420
TGCACGCCTG TAATCCCAGC ACTTTGGGAG GCCAAGCTGG GTGGATCACT TGAGCTCAGG 480
AGTTTGAGAC CAGCCTGAGC AATATGGTGA AGCCTGGTCT CTACAGAAAA CACAAAAAGC 540
AGCCAGACGT GGTGGTGCTT GCCTGGAGTC TCAGCTCCTT GGGAGGTTGA AGTGGGAGGA 600
TTGCTTGAGT CCTGGAGGTC AAGGCTACAG GGAGATGAGA TGGCATCACT GTACCCTGAC 660
CTGGGGGACA GAGCGAGACC CTTTTCATGC CCCGGGACAT TTGCTGGTGC TGTTTCTTCT 720
GGTTGGCATA CCCTTTCTGA GGACTGCCCA ACTTTGCTCT GAGCCAAGGG TAGAAGGAGA 780
TGTGGCCCTT ATCCATTCCT CCAGCTTTTC CCCTACCCTC AGAGCTCTTA GGCAGTGGGT 840
ATGGCACCTT GGAAGCTGCA GCAGGGTCAG GGCACATTGA GTGACTAAGC ATAGCAAGTA 900
CCAGGTGGAC GGGGCAGAAA TGCCAGAGGT GGGAGCTGTG CTCTGCCTTA GGTCCTCTAA 960
GTTTGTGTGT GAGTACAGCC AGTGTCTGAC CTCTTGGAAA TGTGACCAAG ACCACAGTGA 1020
AGACTAGATG ATGGTCCTGT GCTTTCCCCA CTTGTTGATT TCTTTCTTGG CAGAGTATGA 1080
ACTAGGACAC ACCTTGTGTT CCTGTGTGGC AGGCGTGACT GGATCCAAGC TTTCTCCCCT 1140
GCTTGCTTTA GATTTTCCTG GACATTTCTT AGTCATCCCA GCACTGAGCT TCTATTTTTA 1200
GTGCCACTAC CTCCTAGGGG ACCTAAAATA AAGCTGGCTT AGCTTCCTGC TCCCTCATTG 1260
GCTTGAGTGT TGGTCACAGA GCGGAGGATT GGCTGCGTTC TCACTCTTTC CCTACACGAT 1320
TCCTCCCCGC TGGCTCCTCT GGCTTTGGGC GAGGTCACAC GGACTGGAGT GAGCTAGCAC 1380
TTACCATGTT GAGCTGAGGG CTTTATCATG TTCCTTTAGA GAAGCTTCAC AACCACCGGC 1440
ACTGTCAGGT TGCCATCCCC ATCTTATAGT GGAGGAGGCT GAGGCCCTAA GAAGGGCAGT 1500
GACTTGCATC AGATCCCACC ACTGCGAATG CTTGTCTGCT GGGGTGGAAC CCACCTCCTC 1560
ACTGCTTTGG TTCAGAGTCC TATTATCAGG ACAGAGGGAG TGGGCTCCTC TACAGTTGGG 1620
GCCATCCACA GAAAAACATG TGGGTCTGCA GTCAGGGGAT CTGCAGCAAG ATGTGGGCTT 1680
CCCTACTTGG AAGCAGCCTA GCAAAGCCCA AGCGGCTCTC CCATCTGGGG CTTGGGTTTT 1740
CCATCCAGTA TCCTTACAGC CATGGTCTCT AGTTGGGAGG GGGCCTCCTC TCAGAGACCC 1800
GAGAGAGACA GCTCCTTAGG GTAAAAGCAA TGCTGGGATG AGGGGATATG AAGGGATGAC 1860
ACGTTTCCCT TCACAGCCTC CATCCCCTCT TCCCACAACC CTCAGCTTTC CCTCTGATCC 1920
TTGAACTCAT GTCCCCAGCT CTGAAGTGGG TAGGAGTCAC TCCCATCAAT GAAGAAATAT 1980
CCTAGAAAGG GCCAGGTCAG GTAATCACCT GGCCTCGGGG AAGTAAACTG CCCCCATGAG 2040
ACTAAGGGAT CACTTGCTGT TTTTGGCAGA GGAGGGCCCT TGGCTGGGTA CAGTGGCTCA 2100
CGCCTGTAAC CCCAGAACTT TGGGAGGCCA 2130
|
