| Tag | Content |
|---|
EnhancerAtlas ID | HS188-03191 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr12:109982340-109984000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr12:109983668-109983681 | AGCAGCTGCCCCC | + | 6.03 |
|
| | 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 |
| GH12I109544 | chr12 | 109982612 | 109983475 |
|
Enhancer Sequence | TCTAACTGAC AATCTTGGGT AAGTCGGCCC TCAGCCTCTG CATCTCCCAC CACAGACCAA 60
GGCTCCCAGA TCCCCCCAGC CCATGCACTC CATGTGGTCC CCTCTGTGTG CCTGGATACA 120
TCGGGACTCT TGGGTGTCAC TGGGGATTCC TGCCCTGCCA CATGGGGTAA GCTACTGGTA 180
ATTACTCAGC TGTGGGAGCT CCTGGTCATC AGCCTTCAAA CACAGAAACT CAGGTATTTT 240
TCCCAGCAGA CCCTGACCAG CCTCTGTATT TCTCCATAAC GCTGGTCGGC TGGGCACAGC 300
GATCTTGGCA ACAGATTTTG CGAAATAAAC TTGGTCAGTG GATCCCAGTC AACAAAATGT 360
TTTTCCATCT GTTACCCACT TCCTCCTGCC TGTGAAGGGG CAGTGCTCTC TCCTTCTTAT 420
AGGTGAGGCT CTGAGAGGTG GAGTGAGTGA CTTGCCCAGG GACTCAAAGC CAGGATATGA 480
GGAACTGGGA TGTAAGCCCA AGCCTTTGAC CAGGAAGGTG ACCTCACTCA CTCACTTGCC 540
TTCCCTGATC GTCAGAGGCC TGGACAGAAG CCTTCTGTCT CCCAGAGGGG CTAGTCCCAC 600
TGACTCTCCT GACCTGCTCC CATCCCACTA GGGACACTGT CCAGGGGAGG GAGCACACCC 660
CATGTGGGGC TTGGTGTGAA GTCTGCTGGG TGGCTTTGTC ACATTGCAGA TGGTGCCAGA 720
TGAGCCGGGC CCCGCCCAGG AAGCCAGACT GCCAGGGAGT TCAGACTCAG CCAACAAACA 780
GACCCACAGG GCCTCCTGTG CCCCAGGCTG GGTGCTGAGT TACAGCCGTG CACACGGTGG 840
ACGTGATCCC TGCCCTACAG AGCTCACTCT CTGGTGGGAA AGAGTCAGAA CTAATTCAAG 900
GAGGAGGTGT ATGGCCACAT CCTGTGATCA GCGTCCCTGG CATCTAGTGC TGTGCTATTC 960
TGATGCCCAC TCAAGTGGGG AAAGCTGAGG TCAGGAGCTG GTCATTCCCA TGCCCAAGGC 1020
CCCAGAGTCA GTTAAGTGGC AGAGCCAGGA TTCAAACCCT GGTCTGCCAC ACTCCAGAGC 1080
CCTCACTCGG TTTGAGCAGG CAGAAGAGGG GTGGGAGAAC ATTCTAGGCA AAGGGCTCAG 1140
CTTGAGCCAA GCCCCAGGGG CTGCTCTGTC CCTTATCTGG AGCCCGCTGC CTCCACTGCT 1200
TGTCCCACTT ACCCTTGCCG GGGATGCTGC AAACTGACAG ACACACCCAT TTTGCCAGTG 1260
AGTTCCCACA GCATTTTAAA GGACTTCTTC AGGACCCTAG AGCCCTGGTC TCCCCAAGGC 1320
TGCAGAGCAG CAGCTGCCCC CCAGGCACAG AGCTGAAAGG CAGAGCTGGA TTTCAGGGTG 1380
TGCTGAGTAA AGGGCCGATC TACCCTGCAC TTTGGAAGCT CACCGGGTAG AGGGAGGCCA 1440
GAGGAATTTC AGGGACTCCA CGACTTCCTT AGCTTATCAT TCATGTCCCA ACAGGCTGCA 1500
GCCTGTCTCC CTACCAGCTA AGGCAGAGTT GCAAGTGGGA CAGAATCAGT GCCCACTCCA 1560
AACATGGCTC CTTGGCTGCA TCTGGGAACG GGTTCCATTA GGTGGTGTGT GGAGGGTCTC 1620
AAACATCTTA ACAGTGATGG TGAATGCGCC AGTGCCTCTG 1660
|
