| Tag | Content |
|---|
EnhancerAtlas ID | HS095-10898 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:3553140-3554180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr16:3553835-3553856 | TCACACTTTCTGTTTCATTGT | + | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr16:3553515-3553530 | TGAACTCCTGACCTC | - | 6.22 | | STAT1 | MA0137.3 | chr16:3553783-3553794 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr16:3553783-3553794 | TTTCCCAGAAA | - | 6.32 |
|
| | 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 |
| GH16I003503 | chr16 | 3553380 | 3554398 |
|
Enhancer Sequence | ACTTTTGTAT TTTTATTTTT ATTTTATTCT TTTCTTTTTT TGAGATGGAG TCTCGCTCTG 60
TCACCCAGGC TGGAGTGCAG TGACGCGATC TCGGCTCACT GCAAGCTCCG CCTCCTGGGT 120
TCACGCCATT CTCCTGCCTC AGCCTCCTAG TAGCTGGGAC TACAGGTGCC CGCCACCACA 180
CCTGGCTAAT TTTTTTGTAT TTTTAGTAGA GACGGGGTTT CACCGTGTTA GCCAGGATGG 240
TCTCAATCTC CTGACCTTGT GATCCACTCG CCTCGGCCTC CCAGAGTGCT GGGATTACAG 300
GCGTGAGCCA CTGTGCCCGG CAACTTTTGT ATTTTTAGTA GAGGTGGGGT TTCACCATTT 360
TGGTCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCTA CCCTCCTCGG CTCCCAAAGT 420
GCTGAGATTA CAGGCGTGAA CCACCCGCGC CTGGCCTTTT TTGTTTTTGT TTTTGAGACA 480
GGGTCTCACT CTGTCACCCA GGCTGGAGTG CAGTCACATG ATCTGAGCTT ACTGCAACCT 540
CCTGGGCCCA GGTGATCGTC CCACCTCAGC CTGCTGAATA GCTGAGACCA CAGGCATGCA 600
CCACCACACC CAGTTAATTT TTTTTTTAAT CTCTGTATTC ACATTTCCCA GAAAACAGTT 660
ACAGAGTCCC TTTGTGACTT TGCTGTTTCC TGTGCTCACA CTTTCTGTTT CATTGTCTTG 720
CGAAGTCTGA CCTGACTTGC AGTACCTAGG TAGGTTATTT GTGAACATTG ATGGACCATT 780
TTGAACATGG ATCTTCAAGA AGAGTGCAGA CAGACCTTAA ATAACCAGGA AGCACACTGA 840
ATGTAGATCT TGGTACATAT GGGAACTCAA CAAATGTTTG TGGTGTTCAT TTCCAAGTCC 900
TGCTCTCTTG AAAGCACTAA GGCTTTTCCT GAGGTGACCC CAACCTATGG ATCAACAAGT 960
ATTAGTATTA CTGTTTCTTA ATCTGTTTTA TAGTAAATCT AAATATGGTT GTATAGTTCA 1020
ACCACTCTAT TTAAGATTTC 1040
|
