| Tag | Content |
|---|
EnhancerAtlas ID | HS095-25469 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr6:7332200-7333510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr6:7332428-7332443 | GGAGAGCAAAGGCCA | + | 6.15 | | Nr2f6(var.2) | MA0728.1 | chr6:7333402-7333417 | TGAACTCTTGACCTC | - | 7.64 | | RARA | MA0729.1 | chr6:7333399-7333417 | TCTTGAACTCTTGACCTC | - | 6.45 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 7332397 | 7332555 | | chr6 | 7332549 | 7332800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I007332 | chr6 | 7332233 | 7332833 |
|
Enhancer Sequence | CCAATGCTTC TTTTGCTTAC TCTAAAGTAA CAGTCTTCAC TGTGAGGCAT AAACAGTCTC 60
AATTCATTAG GTATACTGTA CTGTCTTAAT ATTAATCAAT CCTTTAATCT TCACTCAAAA 120
GCAGGGCTTC TCCTCCCCAT CTATCAGTTC AGGTCTGTAG CTGATGGACA CCACTGTCTT 180
TGGAGGCCAG TTTCCCCTTT TTGCTCATTT CCCTCTCCAT TTGTAGGAGG AGAGCAAAGG 240
CCACAGGACA GCTCATACTT GGCTGGGTGG CTTCAGAGTC TCAGCTTGGC AATTGGCTAA 300
TGCTGATTCT TTCTCTTTGG AGCTTGCCGT TGCTGGGGAT CTCTGTCCTG CAGTTCCCAG 360
GACCTACGCG GAGGCATTTC TCCTCTGGGT GATCACTCGA TACTCTATCA GCCCCGAAGA 420
ATCTGGCATT CTCTTCTAGT TTCTTGCTGC TTCCAGGCCT CCTTGGGCAG AGCTGAAGAT 480
AACTCAACTC TCAACTGCAT GGTTCTTAAG GGATTTTCAC ACCCATTCTT TGTCTCAACA 540
AGCTCAGAGA GAAAAGCTAT CCAACACAGC CCCTCTGCTG AGCAGCCACA GCTTGCCTTA 600
GTTTTCTTAG GCATGAATGA ATCACCAGTC CTCTGTGTTT CCCAACTTTT AGGGAACACG 660
TTTCAAAGCT CTTTAGGTGA TTCCCTGGAA ACTCCTCATA AGGCTTTAGG TAAAAGAGGT 720
AGAATTACCT GGGAGACAGG AACTCATGAC ACGACAGATT CGAAGAAATC CTTCTCCAAT 780
CTTCCCTACT CTCCATACTT TTATATCTTG GATCTGGCCA AGAGATAGGA GTCATGGAAG 840
GGGTTCTCTG AAATCATTTA TTTCGGAAAC TCTGCACATG GGAAAAACTC ACTCTCACTT 900
TGGGAACTGG TAACAGTGTT ATTAGCACCT AAGGAACTGG GCTAGAAAGA GTCTCATTTT 960
AACATACTGC TGTGTTCTTT TTTTTTTCTT TTCTTTTCTT GAGATGGAGT TTTTGCCCTG 1020
TTGCCCAGGC TGTAGTGCAG TGGCACGATC TCAGCTCACT GCAACCTCTG CCTCCCGGGT 1080
TCAAGCGATT CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA TTACAGGTGC CCACCACCAT 1140
GCCTGGCTAA TTTTTGTATT TTTAGTAGAG ACAGGGTTTC ACCATGTTGG CCAGGCTAGT 1200
CTTGAACTCT TGACCTCAAG TGATTCACCC GCCTCAGTCT CCCAAAGTGC TAGGATTACA 1260
GGCATGAGCC ACCGTGCCCT GCCTATACTG CTGTGTTCTT AATCAACCAC 1310
|
