| Tag | Content |
|---|
EnhancerAtlas ID | HS092-03977 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:181148680-181150150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:181149515-181149527 | GTTTGTTTGTTT | + | 6.32 | | REL | MA0101.1 | chr1:181149149-181149159 | GGGGATTTCC | + | 6.02 | | RREB1 | MA0073.1 | chr1:181149927-181149947 | TGGTGTGGGGTGGTGTGAGG | - | 6.5 | | RREB1 | MA0073.1 | chr1:181149937-181149957 | TGGTGTGAGGTGGTTGGGGG | - | 6.99 |
|
| | 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 |
| GH01I181179 | chr1 | 181148337 | 181150297 |
|
Enhancer Sequence | GACTGCAGCA TCAGTTCCTG CATGAGTTTC CAGCCTGCTA GCCTGCTCCA CAGATCTCAG 60
ACTTGCCAGC CTCCACAACT GTATGAGCCA ATTCCTGAAA TAAATTCCTT TATACATATA 120
TGTAATATGT ACACATACAC ACATCTATGT CATCTAGATT TAGAGCTAAT CTAGCTCCTC 180
CTGGCTCTGT TTGTCTGGAG AACCCCGACT GATACTGATG TGTTTATTTG CTTATCATCC 240
TCCCTACCCC AGACGGAGGC TCTCTAAGGG GAAGATCTTT TGTCTGTTTC CTTCATGCTG 300
TGTCTGAAGT GACCAGGACA GCAGCCGGCA ATAGGACGTG CTCAGTCGAT ATTGTACAAT 360
GGATCTTCAT AATTCTTGCT TATTTGTGTG GTTGTTATCT GTCTGAAATT CAAGAAAGAA 420
GGACATGAGA AAAGAAAAGG ATGAAAGCAC ACTGGTCTTA TCTGAGGCTG GGGATTTCCC 480
CGTTGGGCCC AGTGTTGTGG ATTCTGCAGT TGAGTTGTGT CTGTTTGCAG CTGAAAGAAA 540
GCTGTGGCAG TGAGGAGAGG TTGCAAATTT AGAATCAAGT TCAAGTTCTC CTAGCAACAT 600
GCACACCCCC GCTGCTGGCT GGTGTAATCC AAGCACCAAA CACGTGCAGC TGGGGCAGTG 660
CGTGTTGCTA GGAGAACAAT GACTCTCTTG CTTCCAGAGC TGGTAGGTGA CTGCGGTATT 720
ACCAGGGGCG CACAAAGTGG GTGTTGCCCT TTGTTTCCCA AGTAATTGTT TTAAAGCAAG 780
GTGAGGAGGA GCCTGGGGAA GGGTAGAATG AGAGAAAGCA TGAACCCTGA TTTGTGTTTG 840
TTTGTTTAGG AACTAGAGGT TAGTGAAAAG CCTCTTGTTT CAGAATGTGT CCCAAATGGG 900
TTTACAATTA GTGACAGAGT CTGTAGGAGC TTATGAAACA ACCAATTCCC CACACTGTTT 960
GGCTCTCAGC ATCCACAGAC CATCTGGATC AGCTGAGCAT GAAGTGTGGG GGCGTGCATT 1020
GGGGGTGGGG TCCAGAAACA AAAAAGATCA AGCTGGCATC GGTTGGGGCG GGAGAGGGAT 1080
TTGGGTTTTC AGATTTCCTT TCGCTTAATT ACATTCGCAG GCTGTCCTGA TCCTCATTCC 1140
CCTTCCCCAT TGTTTCTGCC CTGTCAGCGG GGTTGACTGG CTGAAAACAG ACCACCCGGG 1200
CAGCCAGAAG AACTGTGCCT GTCCCGGCAG CCCTGACTCT GGACAGGTGG TGTGGGGTGG 1260
TGTGAGGTGG TTGGGGGACG GGAGAACAGG GAAGCAGGGC CAAGGACAGT AATATCCCTG 1320
GCCACTCTTC ATATATGTAG TCACCAATGC TCAAAGTCCT CCATGCCCCC ACTTCCATCC 1380
TGCAAAGGAG GAAGCTGAGC TGCCAAGGAG TGGCAGAGCT GAGAGCAGCA CCAGCTCCGT 1440
CTCTCCCGAA GACCACCTTC TTTCTCCCAT 1470
|
