| Tag | Content |
|---|
EnhancerAtlas ID | HS098-01495 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:39512480-39513940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:39513769-39513780 | GGATGACTCAT | + | 6.62 | | JUN(var.2) | MA0489.1 | chr1:39513771-39513785 | ATGACTCATCTTCC | - | 6.3 | | JUNB | MA0490.1 | chr1:39513769-39513780 | GGATGACTCAT | + | 6.62 |
|
| | 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 |
| GH01I039046 | chr1 | 39512253 | 39514624 |
|
Enhancer Sequence | TCCCCCTCAT CCTTTTATCT ATGGCCAAGC CCTCCTGAAG GGTCTCTTTG AATCGCGTTA 60
CCTCCTAGTT TGACACCAGT GCTCTTATTT CCCTGTGGCA TTGGAGGGCT AGTCACATGG 120
CACTGTGGCC AAGGAGAAGG ATGATGTTCC AGGCCAAACA CATCTGCAAA TGTGTTGAGC 180
TGGTGTCCTT GATGACAAAT CAAATTGTTT TGTGTTTGGT TCCCCAGAGG CCTGAGTACC 240
TCAGAGAAGC CAAGGTTCCT GCAGGAACCT CGTGCCTGCT GTCCACGTTG GGCTTCATTT 300
TATCAAAATA CAGCAAAGAG CTCATCATTT CTCAGCTCCT GTCGGAAGCA ACAGTGGCTG 360
TTCCTGGACA CAGAGCTGCA GACAAGGAGT GGTGAGGATT CAGGCAAGAG AAGATGGGCA 420
GCTTCCCCTT CATGCTTCCC TCTCAGGAAG AAGCCAGGGT GCCTGGGATC AAAGAGGCTA 480
GGAGGCTGGT GAGGCCTCCT GTCCCTGAAA GCGGTCAGTG AACCCAAAAG TTGAAAAGCC 540
TCTGCTTTGA GAGTGGTTCT GCTGCCCTAC TGGTGCTGAC AGTTTTAGAA ACTGACATGG 600
CAGAGCTGAC CAGGCAGACT ATATTTTTAG GACTCTGCTG GGGCCTATTG AAACGTCCAC 660
ATTACTCAGA TCACCAATCT GGCTGGAGCT ACCAACACAG CATTCTTTGC TGTTTTAGAA 720
TACAAAGCTA CCTCCCCTCG GGGCTTCACT TTGCAGCCAC TGAGAATCCA AGGCTTCGCT 780
AAATTACACG TTTCCATGGT CCCACTGGCT TGCTTTGCAG GGCTTCCACA AGAATGGGCT 840
GGGAGCGTAA CTGAGTAACT GAGTCATGAT TAGGGGTTAA TTAAGAGGAG AAATGGGCTA 900
GCTGTTTCCT AAGATAAGGG AGGGGAAGTT TTTTTAAAAA CTGTAACTGC TCAGAACAGT 960
ATGTGCTAAG GCAGACTTTC TGTGCTGGGA GACAGAACAC TTCTGCAGTG ATGTAGCAGA 1020
ATCCTTAAAG GATCCTGCCA ATGACTCTTT TTTTCTGGTG TCACATCCAA TCTTTGCTGC 1080
AGCCAACACT TCCTGGAGAT GAAACACAAC TTCAATACAG AGATAGCAAG TTCACACTCT 1140
GGCAGTCATG CAAGGATGAG TGATGCGGGC CTTTTCTAAG TGAGTATGAA CGGGTGGGAC 1200
CTACGGTAAA TTCAATGCAG TATAATCCGT CTACGGGGCA GTGGGCACCC AGCAACAGCC 1260
AACTGTTACC AAATCAAAGT GCAGGCCCAG GATGACTCAT CTTCCAGCAT TTCATGAGCA 1320
ACCAGAAGTC TACATTTCTT TGAGAAAAAA AATTTTTTTG AGACGAGGTC TTACTCTGTT 1380
GCCCAGGCTG GAGTGTGTAG CTTCTACCTC CCGGGGCTTA GGTGATTCTC CCACCTCAAG 1440
TCTCCCAAGT AGCTGAGACT 1460
|
