| Tag | Content |
|---|
EnhancerAtlas ID | HS024-14084 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr6:109750060-109751560 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crem | MA0609.1 | chr6:109750522-109750532 | TTACGTCATA | - | 6.02 | | FOXP2 | MA0593.1 | chr6:109750291-109750302 | AAGTAAACAAA | + | 6.62 | | OLIG2 | MA0678.1 | chr6:109750272-109750282 | ACCATATGGT | + | 6.02 | | OLIG2 | MA0678.1 | chr6:109750272-109750282 | ACCATATGGT | - | 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 |
| GH06I109428 | chr6 | 109749967 | 109750980 |
|
Enhancer Sequence | GATAAAGAGG ATATATTGGA AATCATGGCT GACTTAGGAA ATGGACTTAC TGTCCATTCA 60
GACACCATTA AACTTCCCTG CGCATCAAGA TATTATCTTT ATGAGATAGT CCAGAATAGA 120
TAGTTCTGAA AATGCCAATA AGAGTTCAAA TGAATGCAAC ACAAGGTAAT GTCCCAGTCA 180
TCTAGCAGCC AAACAGGCAA GCATATTTAT CTACCATATG GTTCTAACCG GAAGTAAACA 240
AATCCCTGGG TTTTATTCAG GAAGAAAAGT CCACCCTCTG TGCAAAAAAA ATCTATTGTC 300
TCTGGAACGC TTCATGACTA TCCTCTATCC TCACTGCCAC GAATTATTTC GGGCTTTCAT 360
TATGTCCAGC CCATGCTGCT ATCCAATCCC CTGCTCCCAA GCTCTCCCCT ACTCCAGCCT 420
GCTTCTGCAC AGACCTAAAC ATTTTTCCAG AAAAACAGAG GATTACGTCA TACTCTTTTA 480
TGGAAAGCTC TGTTGGTTCA GTTTCCTTCT GGATAAAATC CAACTCCTTC GTTCAGATGG 540
ACAATAAATC ATAACCCAGC CTCAATCTTT CTTTAGGATC TATTGGATTT TTTTTTTCCT 600
AATTAAAATC TGAGTACCCT TCCTATCTGG GGAACTCCTC ACAGGGTCCC ACCACCTTCA 660
CTAGAACCTA AAGGGGCCAG ATTCTCCCTC TCCCCATGCT GAGAGCACCA GGTTTTGGGA 720
ATATGACCTA GCCTTGCCAG CTAGGTGCTC CTGCCTGGGC TTAGGTCTCC AGGGAGTGAT 780
GAAAAGACAC TGAAGCATTG AACAGTTAAT CTCATTGAAG GTGGAGGTGT GAACAAGGGC 840
CAGCAGTGCC ATGGCAGTTC CCTGGCAGCA CATCCCTGCA GTGTGACTCT GGCCATGTCT 900
TCCTGCTGCC AGGCCTCATT GGTTCCCGCC TGTTTTCCAA AGCTGTTGTC CAGCTTTCCT 960
GTCAATTGTG AGATAACAGC ATCCTTTCAA TACACACCTT TTCGCCTTCG ATCAATCAGA 1020
GGAGCTTGGT AATGCTGGCA CCAAGAATCT TGACTGAAAC TCATCTTCCC AGCTTCTTTC 1080
CCCACAAATT CTGGCCTCCT TGCTGTCCCC CTGCCATTCC CAGGGCATGT ACAGCTAGAC 1140
TCCTGACCCT TTGGGAATTA ACTGTTTGAA CATTAAATGC CTCCCCACAC CCCAGAGTTT 1200
CTAGCATTGT CAAAGTGCAC TGTTTATTCA ATCAAACATG CACTGAGCAC CTATTATGTT 1260
TCAGGTCTGT TTGAGCAGTG GTTCAACAAG GATGAATGAG ACAAGGCCTT TACCTATGCA 1320
CAACTCAGAT CTTAGCATTG GCTCACTGTA GGCACAGGCC GCCATGGGCA TGAAATGATT 1380
TTCTGCACAA TGCAGTTGTT GCTACAAGAA GGTTTCTGAG CAGGACTGCA AAGTACCTCC 1440
ACCCCTACTG CCATCACATC CTGATAACTA TCTCTCATCC CTGGACCTCA TGCTTCATGA 1500
|
