| Tag | Content |
|---|
EnhancerAtlas ID | HS104-57051 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr8:17204920-17206460 |
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 | chr8:17204968-17204981 | GAAGCTTCTAGAA | - | 6.28 |
|
| | 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 |
| GH08I017347 | chr8 | 17204976 | 17209403 |
|
Enhancer Sequence | GGCTATGTGC TCACTCTGAT GAAGCTGGCA TTGCTCCAGA TATTTTTGGA AGCTTCTAGA 60
ATCTGACTGA GACCCTGCTC TACCCCCCGG CTGTAGGTGC AGGCATGTGG ATACACACTC 120
ACACAATCTC CTGTGTTTAT AGCCTCACTC GGCTTTGAAT CCAGAAGTAT ATTATCTAGC 180
TTAAAAACTA AAGTTTCTCT CTCACCTTGC TAGAACCAAA GAACATTTTG TTTTTTTAAA 240
CCACCTTTTT TAAAGGTGGT TTTTTGCTAC CTTTTAAAAG TGGGTGCCAA AGACCATTCT 300
TGCTCATCCG AATTTGTTTT CCTATCCTCC GCAGAAATGG AACTCTAAGT TTTAGCTATT 360
TTAATGGCCA CCCATAACAC TGTACTTCCA CACCTGCCCT GTGCAATTCT GATGAAAGGG 420
AGGTGTCACG TGGCAGTTTT TGGAAGCCTT CCTTAAAAAG CTGGGCACAC AACATTAGCC 480
CTCCGTCACC TGCCACCTGC AGTGTGTGGG TGGTGACTGT ACTGAAGTGA CCTCTTGCAC 540
CAGGCAGGCC ATGGCCAAAT CCAGGTGGTG GTAGAGCAGA AAGGTAGAAG GAGCTTGAGT 600
ACCTGAAGGC TAAGTGGGGT GGGGCCAGGC TACCAGGCTA GGACTGCGCA CCCTGGTAAT 660
TTTACGCAAC AGAAAAAAAT TGTATCCTCT TAGAGCCACT GTTACTTAGA GTCTCTATTA 720
CAGACAAACC CAATTCTGGC TTTTATAAAT AATATTTTAA AAATAAAACC CATGCTCTCT 780
ATAACCAAAG ATTTCTTATA CTGAAGATAC TCAAAAGAAC ATGAAATTTA AAAACAGGTA 840
ATAAGGCCGG GCACAGTGGC TCACGCCTGT AATCCCAGCA CTTTGTGAGG CCGAGGCAGG 900
TGGGTCACCT GTGGTCGGGA GTTCAAGACC ACCCTGGCCA ACATGGTGAA ACCCCTTCTT 960
TACTAAAAAT ACAAAAAAAA AACCCAAAAT TAGCTGGGCA TGTTGGCAGG TGCCTGTAAT 1020
CCCAGCTACA AAAGAGGCTG AGGCAGGAGA ATTGCTTGAA CCTGGGAGGC AGAGGTTGCA 1080
GTGAGCCGAG ATTGCACCAC TGCACTCTAG CCCAGGTGAC AGAGTGAGAC TCTGTCTCAA 1140
AAAAAAAAAA AAAAAAACGT AATAGAGAAA AAGAATGGGC CATGGACTTC GGGGGCTTTT 1200
CTAAAATAGG CATGCCACAG ATCTCCAGCA CTGAATAAGC AAAGAGATTC CCAAGGTGCC 1260
CACTTAGGAC AGTATTCACT TGCATGATTA GCTTTAGGGG TTTTCTGAAT CTATTGAGTC 1320
ATTTTCTGAA TCATTACATT ACTGTCAAAT AAACATAGGA AGTCTACATG AGATAAGGAC 1380
TTAGCATAGT TGTATCATGT CATACCATGC ACAGGAATAT CCACATACCT TCTGAAGAAT 1440
TCAAACACAC ACACACGCAC AGCAGAAGGC AGCTAGAAAA TGCCTGCTTA TGATAAACTA 1500
GAAAAGCAAA GTGTAAAACA AAAACACGCC TCGAGACTTA 1540
|
