| Tag | Content |
|---|
EnhancerAtlas ID | HS165-14860 | Organism | Homo sapiens | Tissue/cell | Ramos | Coordinate | chr8:10955920-10957570 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr8:10956397-10956410 | TTCTGGAACATTC | + | 6.67 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 10956694 | 10956827 | | chr8 | 10957216 | 10957311 |
| Enhancer Sequence | TTTAGCAGTC TCGAGTTTTT CCTGACGCTA CTAATGCTGT GTGTACTTCT CACTCACGGA 60
ATACGAGGTG TCAGAAAGCA CAATTTGGAA CTGTATCTTG GTAATTTCAC AACTGGGACA 120
GGAACTCTTG TCTCATCAGA ACTATGCCGA AAAGCTTTCT CCATAGGCTA GGATGACTAT 180
GTGGTCATGC ATGTTTGAAT TATGTTCCTG TTTCCAATTA AATATCCCTT ACAGAAAGGT 240
TCAAGGTACC TCTTTTATAG TATGTGGAAA GTTTATTTTT GAATAATTTA TTTATTGCTT 300
GCACAAGTGA TAAGAACCTC TTAGAAATCT TGTTCCCTTA ACTATTAGTC TATTCACATT 360
CTTGGACGAA TAAAAAGCTT TACTTTCTTT TGAATCTTAA GTGGGGCTAG GAGGGAGAAA 420
TACAAATTCT GTTCTGTTTC AAAAGTTGGT TTTAAATAGA CTTTGCATCT TGGAAACTTC 480
TGGAACATTC CCCCATGGAA AAAAAAATGA TTATTAGGTT CTGAATTGAG CTCATGTAGG 540
TGTAACATAG AAAGGGGTAT TAATAAGAAT TTTCTTTATG GGTATAGTCT AGGAGAATAA 600
TGAGCTTCTT CCCCCTTCCC TAGCCCCTGG GCACCCTCAA CGCCCCACCA GGTAGGCACG 660
CTGTCCATTT TCGCCCTCCT CTGTCCAAAA AGCAGCAGCT GCCACCTCCC TGGGAAGAGG 720
CAGGCACCCT ATTACAGCTC CCGCTCCACT GAACCACATC TCCTTTCTTC AGATCTCTTC 780
TCTTAGCTGG GTACAGCAGG AGGGCAATCG TCCAACCAAA GTCACATCGA AAATCTGGAA 840
GCTTGGCAAG GCTGTCCAGC TGACTTTTGT CACCCTGGCC TCTAACACAA TAGCCACACC 900
ATTGCTGCTG CCCAATAAAT ACCTGTTAAA TGGCTGAATC TACTAAAACA TTTTTAAAAG 960
ATGATGCTTA TCATTAGCAC AAGTCAACCT CCAACTGGGG GAATTTTAGG CTCTGGCTTC 1020
AAGTGAAAAT TCTGGGAGAG AAGGGGCTGG AGGCAGGAAT GGCACTGCTG GGCAGGGCAG 1080
CCCTGCCTGG AGAGCGAGCT CTGAGATCAG CTCCTCTCTT ACAGTCGCTG GATTTTTTTC 1140
ATAACTCCTT TACTTTCTTT ACTTCTAAAT CCACATTCTT TAAAATCTCC AAGTTTCCTT 1200
GCAACTCCCT AGGCAAGGGC AATGAAGGAT TTACTCATTC ACTCGCTCAA ATATTATATA 1260
GGTATTGAAT TTCTAATGTG TCTCACGCAT TGTTCTAGGT CTTGAAAAAA CAGCCACCAA 1320
CAAAACAAAG CCCCTGCCCT CCCTGAGCAT ATATTTAGCG GAGGAGACAA AACTATAATG 1380
TGAGGTCATG ATGGAGGTGA TGAGGAAGTT AAGGGAGACC ATGGCAGAGG TGCCACTCTA 1440
GACAGGCTGG GCAGAGCCCT CTCTGCGGAG GAGACAATTT AGCAGAGATG GAGCCATAAG 1500
CACATGGGGA GGAGCATCCT AGACAAAGCG AGCAGCAAAT GCAAGGGCCC TGAGGCACGG 1560
GGGAGTAGGG CACCCTAGCG GGTTGGGCGC TGGGAGGGAG AGGGGGTGCA GCCAGTTTAA 1620
GTAGGGCTCA TTTTTTTTCT TTTCATTTTG 1650
|
| |
|
|
|
