| Tag | Content |
|---|
EnhancerAtlas ID | HS176-13163 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr14:103046030-103047190 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I102579 | chr14 | 103045483 | 103047619 |
|
Enhancer Sequence | GTGGCGCATG CCTGTAATCC CAGCTACTCA GAGGCTGAGG CAGGAAAATC GCTTGAACCT 60
GGGAGGCGGA GGTTGTGGTG AGCCGGGATT GCGTCATTGC ACTCCAGCCT GGGCAACAAG 120
AGTGAAACTC TTGTCTCCAA AAAAAAAAAA AAAAAAAAAG GAAACTGAGG CCCTGAGAGG 180
TCCAGGGGCT CTCAGGCAGC CAGAGGCAGC ACCTGACCTG GCCCAGGCCC CCTTCCCCGG 240
GAGCACAGAT GCCAGGATGT GTGGATTGGC GCCCTTCTTG GGCTGCTGGG CCCCGTGGTC 300
TGCTAATTAG TCACATCATT TTTGGCATCG CACACAGCCT CGGGAACTGG AGAATGTCAT 360
TGTCAAAGTA TTTTTGAATA TTTGCCTTCT CAGCAAGAAG ATGAGAAAGC TGTGAGGACA 420
CTCAGTCTTC CACGGGGTGG ATACTAACCA AAATCACAAG CAGCTTGAGC TGGAAGGACC 480
TGGGAGCCGG GAGAGATGCC GGAGGAGTCC CGCGCGCTGC CTGTCACAGC TGTGTGACTT 540
CGAGACAGGG CTCTGGCCCC CTGGGCCTCA GTGTCCTCCC CTGGAAAATG GCTCATTCAT 600
TTCTCAGGTG GGCATGAAGT TGCTATGTGC CACGCACTGC TGTAGGCTCT GGGGAGCAAA 660
ACAGGCAAAA ATCTCTGCTC TCACAGGCTG CCATCCCCAG GGGGGCCATA CCATAGAAAT 720
CAAATCAGAT ACACCAGGGG TGACACATAG AAGGGAGAGC CCAGGGGTGG GGCTGTCAGG 780
GATGGCCTTG CTGAGAAGGT GACATGCGAG TGAGAATTTG AAGGGGGCAG GAGGGAGCCC 840
AAGGGGTGTC AGGGGAAGAG CCCTCCAGCA CAGGGAGCGG CAGGCACAAA GGCCCTGCAC 900
TCGGGCAGGA CTGGGTTGTT CCAGGAGCAT CAGGGAGGCC AGGCGGGCTA GAGCAGGTGG 960
TGACTCAGGG AGGCAACATG ACAAGACTGG GTCACAAAAG GCCACTGGAG GCCTGCTTGC 1020
TGCTTGTGGA GGGCCTTGTA AACTGCTGGA AAGCCTTTCT TTTCTTTCTA TTTTTGTTGT 1080
TGTTGTTGTT GACAGGGTCT CCCTCTGTCT CCCAGGCTGG AGTGCAGTGG CTAGAGCTCG 1140
CTGTTACTTC AAACTCCTGG 1160
|
