| Tag | Content |
|---|
EnhancerAtlas ID | HS176-11666 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:80166810-80168480 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr13:80168222-80168237 | CAGTGTGGGTGGTCA | - | 6.03 |
|
| | 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 |
| GH13I079592 | chr13 | 80166686 | 80168863 |
|
Enhancer Sequence | GTTAAGCCAC AAAGAAATGG ATGACTGTCT CCAGAGGAAT AGTAGCTTGA ATATCAAAGT 60
TATTCTCTTT CTCTCTAGAA TCTTGGCTTC TCTCAACATG GGACTCTTGA TAGTCTTGAA 120
CTTCAATTTC TGTTTCTCCA GCCCCATAGG GTTGCTAAAA GCTTTGCTCA GCTTCTCAGT 180
CTCTCTGCTT AGGCTTAATT TTTTCTTCTT TCAAGGATCT TTACCCCTGA AATTTGACTA 240
CTTTTATAGT TCTTCAATGC CATTAAACAG GGTTGTGTGT TTGTGTTTGT TGTCCTTCTT 300
TTCTAGTTTT TCTAAGACTA ATAGAAGCAT TGCTCTGCTA TAAGTCAGAA AGCAAAGTCC 360
TTCCCTTGTT TTAGTTACCA CAGTTGGAAA TATTTTATAG TTTTGCAATA GACGGAATGG 420
TTATGTCCTC CCCCTGCCCC CTGCCCAAAT TCCTATGTTG AAATCCTAAC TCCCAAAGTG 480
ATGGCATTAG GAGGTGAGGC CTTTGGGAGG TGATTAGGTC ATGAGAGCAG AGCACTCATA 540
ACTAATTAGA GATCATAACT AATCCCTTAG TGGGATTAGT TCCCTTATAA AAGAGATCCA 600
GAGAGATCCC TCTTACCCTT CCACTATGTG AAGACACATG TGAAGACTGC CATCTGCCAT 660
CACCAGACAG ATTTGGTGTC AGGCGAGGAA GTGAGACCTC CCTAGACTCC ACACCTGTTA 720
GCACCTTGTT CTTAGACTTC CCTCCCTCCA GAACTGTGAG AAATGAATTT CTGTTGTTTG 780
TAAGCCACCC AGTCTAAGGT ATTCCATTAT AGAAGCCAGA AAAGACCAAG GCAAGTTTCC 840
GTTCTTGTCT GCCTTGTTTC CAACCTTTAG TTTTAACCCA ATGAACCAAA AATATACTTG 900
TTCTGACTTT ACTTATAATT TAAATGTAAG AGGGGTTATA TTTGGGATTG TGTATGTGTT 960
TCTAACAAAC AGGAGTTTGT ATTTCTTGCT TCTCCCATTG TGACTTACAG AGTAGATGCT 1020
CTAGAATAAC TGGAATAAAT GAATTTTGTG GTTACCATCT TACTCATGAG AAATTCCCCC 1080
TCCCTGGGAA TCCAGCTGAA TCACTTAGGG TGCCAGCCAG ATGGAGATTT CCTGCCGGAG 1140
ATAAGACAGA CCATCTGCAT CTCTCCTGAG GCAAAGGGGA GAGGAAGCCA AGAGACAACT 1200
CATTTCAGTT TCTTCTGCCG TCAAATGAAC AGGATGACTC TAGTTGGTCT CAAAGTCCCT 1260
TCCAACACTA AGAGTCTGTG CAACTATTAG TGAACCTATT CCTCATTCTT TGGTTTCTTT 1320
TTTGAGGATT TTGTTAAAGA CCATGCCACA TCTGCATCTT TGTTTTTGTC AGGCCATGCC 1380
CATGCTCAGT GGCACTGTGA TAAGGGAGAC TTCAGTGTGG GTGGTCATTT TTGCATTAAC 1440
TCTGTTCACC ATGTATTAGT TTCCTAGGGC TGCCACAACA AATTACCATG AACAATTACC 1500
ATAACAAATT ACCATGGTGG CTTAAAACAA CAGAAATGGA TTCTCTCACA GCTCTAGAGG 1560
CCAGAAAGTA AATCAAGGTG TTGCAAATAT TGTTTGCTTC TGGGGCCTCT AAGGAAAAAC 1620
CATCCCAGGC CTTTCTCTTA GCCTCTGGTG GCTGCTGGCA ATCCTTGGCC 1670
|
