| Tag | Content |
|---|
EnhancerAtlas ID | HS118-17089 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr7:29444840-29446300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr7:29445373-29445385 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr7:29445377-29445389 | GTTTGTTTGTTT | + | 6.32 | | Myod1 | MA0499.1 | chr7:29446123-29446136 | TGCAGCTGTCCTT | + | 6.11 |
|
| | 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 |
| GH07I029405 | chr7 | 29445051 | 29446285 |
|
Enhancer Sequence | CAGTTCCAAC ACTCTGCACC CAGGCTGTTT CTTCTCAGCT CAACCCGATG CTGATAGGAC 60
ACTTTCATTT CTCCATGGGG TCTTTAACGA AGAGTCTGTG TTTAGCAGAG TTTTACTAAA 120
GGTTGGAGCT GGGAGAGCGT AATGATAGCA CAGGGCGCAC ATCATTAACT ACAGTGCAGT 180
GTGTCTGCCC CTGGCAGTGG ATTGGCTGCT GCTTTCTTCC TTCCTGGCAT TGCCTCCCCT 240
GACACACAGA CCCCTCAGCT GTGCCCTCTG GGACCCTCCC CAGCTCTCCT CCCATTAACC 300
ACCCCACCAT CACCACGCCT TTCTCAAACT GCTGCCAAGC CAACTCCCAG AGTCCTCTTG 360
CTTTCTTAGG GCAGGCACCG AAGCCCTCTT TGGTTTCTAC TTTCTTCCTG CAAAACCAAA 420
GAGAGTTACC TTTTCTGGAC TGAAGGCCTT CCAACCTTAC TGGGTTGTCC TTTACAGATG 480
AACTGTTTCA TCAGAGAACA ACCTCTCCCC TCTTGTCTCC CACTCAGCGT TTTGTTTGTT 540
TGTTTGTTTT TTCTTTCTAA ATTATTTTCT TCCTTCCCAG CTGCCCGCCT TTATATCCAA 600
GGTGGTCCTT TCATTGGTTG TTTCACTGTT TCCATCATGT GATCTGCTGG CCTGTCCCGG 660
TATCTTTGCC TAGGAATGAT TCCCTACAAT GTGCTTGAAC AGAGGCCGTG GCCAGGCCAA 720
GGAGTGAATG TCCAGCCCTC GCTTACTGGC AGAAGTCTTC ATACAAGGTT GAGCCTGTCC 780
CGAGTGGTTC TCCCCAGTGC CATGCTCGCA TCTCATGGCT GGTGTCCCCG TGGTGACTCT 840
GTGCTCATCA GAGTGTTATT GTTGTTGCTG TAATTCTGCA ACAGCTCTTA TTTGCTTTTT 900
CTCTAGGACA GAGTTCAAAT TCCTTACAGG AAATTTGCAG CCTGTTTAAG CCTGGGCCCC 960
TTGGAGAAGC AAAGCCTGAG ACTGGGGTTT GGTACAGATG GGGAATTTGG AAAGGCATCC 1020
CAGGGAGAGG AGGAGAAGCT GGGCAGGTAA ATAGAGGAGG AGAGAGGCTG GTATATGCAC 1080
GTTGTGGAGC TGATCACCTT CTCAGGAGCC GGGTAGAACT GCTTCTAAGA GGAATTGAAG 1140
TGGGAGTGTT TAACGCATCA CCTCCTGTCC CCTCTTGGTT GAGGGGTACC TGTGAGCTGT 1200
TAACATTCTC CCCAGTTCCA GGCCAGGCAT GCTGGAGAGC TAGGTGGGTG CCATGGGCAT 1260
CCCTGGCAGC CTGTGGAGTC CAGTGCAGCT GTCCTTTTCT ACTATTGAAT AGAACCTGCC 1320
ACACTCAGCC TCCCCTCCCC TCCCCGCCCT GGCATGCTGC ACACCACCTT TATGAGAGTT 1380
CATCACCCTG TGTCCAGCGT CATTGTTTTG ATCAGTGGTT CTCAAAGCAT GGCCCTCGGG 1440
AACCAGCAGC ATCAACATCA 1460
|
