| Tag | Content |
|---|
EnhancerAtlas ID | HS098-18545 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr14:103045960-103047380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LHX6 | MA0658.1 | chr14:103046331-103046341 | GCTAATTAGT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 103046077 | 103046834 | | chr14 | 103046873 | 103047218 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I102579 | chr14 | 103045483 | 103047619 |
|
Enhancer Sequence | AGTTTGAGAC CAGCCTAACC AACACGGAGA AACCCTGTCT CTACTAAAAA TACAAAATCA 60
GCCAGGCATG GTGGCGCATG CCTGTAATCC CAGCTACTCA GAGGCTGAGG CAGGAAAATC 120
GCTTGAACCT GGGAGGCGGA GGTTGTGGTG AGCCGGGATT GCGTCATTGC ACTCCAGCCT 180
GGGCAACAAG AGTGAAACTC TTGTCTCCAA AAAAAAAAAA AAAAAAAAAG GAAACTGAGG 240
CCCTGAGAGG TCCAGGGGCT CTCAGGCAGC CAGAGGCAGC ACCTGACCTG GCCCAGGCCC 300
CCTTCCCCGG GAGCACAGAT GCCAGGATGT GTGGATTGGC GCCCTTCTTG GGCTGCTGGG 360
CCCCGTGGTC TGCTAATTAG TCACATCATT TTTGGCATCG CACACAGCCT CGGGAACTGG 420
AGAATGTCAT TGTCAAAGTA TTTTTGAATA TTTGCCTTCT CAGCAAGAAG ATGAGAAAGC 480
TGTGAGGACA CTCAGTCTTC CACGGGGTGG ATACTAACCA AAATCACAAG CAGCTTGAGC 540
TGGAAGGACC TGGGAGCCGG GAGAGATGCC GGAGGAGTCC CGCGCGCTGC CTGTCACAGC 600
TGTGTGACTT CGAGACAGGG CTCTGGCCCC CTGGGCCTCA GTGTCCTCCC CTGGAAAATG 660
GCTCATTCAT TTCTCAGGTG GGCATGAAGT TGCTATGTGC CACGCACTGC TGTAGGCTCT 720
GGGGAGCAAA ACAGGCAAAA ATCTCTGCTC TCACAGGCTG CCATCCCCAG GGGGGCCATA 780
CCATAGAAAT CAAATCAGAT ACACCAGGGG TGACACATAG AAGGGAGAGC CCAGGGGTGG 840
GGCTGTCAGG GATGGCCTTG CTGAGAAGGT GACATGCGAG TGAGAATTTG AAGGGGGCAG 900
GAGGGAGCCC AAGGGGTGTC AGGGGAAGAG CCCTCCAGCA CAGGGAGCGG CAGGCACAAA 960
GGCCCTGCAC TCGGGCAGGA CTGGGTTGTT CCAGGAGCAT CAGGGAGGCC AGGCGGGCTA 1020
GAGCAGGTGG TGACTCAGGG AGGCAACATG ACAAGACTGG GTCACAAAAG GCCACTGGAG 1080
GCCTGCTTGC TGCTTGTGGA GGGCCTTGTA AACTGCTGGA AAGCCTTTCT TTTCTTTCTA 1140
TTTTTGTTGT TGTTGTTGTT GACAGGGTCT CCCTCTGTCT CCCAGGCTGG AGTGCAGTGG 1200
CTAGAGCTCG CTGTTACTTC AAACTCCTGG GCTCAAGTGT GTGCCACCAT GCTCTGCACC 1260
CAGGCTGGAG TGCAATGGCG CCATCTCTGC TCACTGCAAC CTCCGCCTCC TGGGTTCAAG 1320
CGATTCTCCT GCCTCAGCCT CCTGAGTAGC TGGGATTAAA GCTGCCTGCC ACCTGCACAG 1380
GTAATTTTTT TTGTATTTTT AGTAAAGACA GGATTGCGCT 1420
|
