| Tag | Content |
|---|
EnhancerAtlas ID | HS176-05930 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:99292230-99293610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr10:99292547-99292568 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | | PLAG1 | MA0163.1 | chr10:99293333-99293347 | CCCCCTTTGCCCCC | - | 7.08 | | Zfx | MA0146.2 | chr10:99292308-99292322 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH10I097532 | chr10 | 99292557 | 99294021 |
|
Enhancer Sequence | CGTCTTTACT AAAAATACAA AAAAATTAGC CAGGCGAGGC TAGTGCGGTG GCTCACGCCT 60
GTAATCCCAG CACTTTGGGA GGCCGAGGCG GGCGGATCAC AAGGTCAAGA GATCGAGACC 120
ATCCTGGCCA ACATGGTGAA ACCCCGTCTC TATTAAAAGT ATAAAAATTA GCTGGGCGTG 180
GTGGCGGGCA CCTGTAGTCC CAGCTACTTG GGAGGCTGAG GCAGGAGAAT CGCTTGAGTC 240
CGGGAGACGG AGGTCGCAGT GAGCCAAGTT CGTGCCACTG CTCTCCAGCC TGGGCAACAA 300
GAGCGCAACT GCATCTCAAA AAAAAAAAGA AAGAAAGAAA GAAAGAAAGC CTTGTTGGTC 360
TTTGGTCTTG CCTCTTATCA CCTTCATCAC TTTCTAATGT TGTGCTCTTA TTTCCGGTGT 420
GTCTCGGGCC CCTACCAAGG GCAGCCTGGA GTCTGGCGCA TCTTCGCAGT CCATGTGGGT 480
AGGACAGTGC CTGGCCCATG GTCAGGGTCC AGGGGAGGAG GAGTGCTTTG CATCCACTTT 540
CCCAGCTGGA AAGCTCTGTT CCTGGCCTTG TGGCTGACTC CTGCATGGTG TTTCCCTGGG 600
TCACCACGGC GACAAGATGC TCACTTGCAA GCAAATAGGA TCCCCTGCCC AGGGCTGCCA 660
GCCTCAGCAG TTCTTGACCT CCAGCTGAGC TGAAACTGAG AGGATGCCTT TTCCACCAGC 720
TGGGAGCTGA GCCCATAGGG CTCCCTCCCT GACCCTTTGG TGACTGTGCT GAAAGCAGAT 780
ACCTCCTGCT GCCCCGGGTT TGCTGCCTTC TCCTCCCCAC CCACTGCTAG AGCCTGTCTG 840
GCATCTATGA AGGGAGGACG TTTGGGCCAA AACAGGTGGT GGTCTCCTAG CACACAGCTA 900
CCAACTGCAT CCTGTCTGCA AGGGAGACTT CTTCCCGGGG CTTTGCTTTC TCCTGGGTTT 960
CAGCACCATG GAAGGCCGCC TATATTCTAC GCCATAGCGG GTGGGAGAAG GGTACGAGGA 1020
GGCTGCTCTT GCCTGGCCTT GGGCTGGTGG AGCGTGTCTG AGGGAATGAG GCCTGATCTG 1080
TCTGCCCTCC CTCTTCGCAG CATCCCCCTT TGCCCCCCAC CTCCACCAAG TCTGACTCAG 1140
CCCTTGCTTG ACACAGATCT TAAGCTCTGG GCTGGGTGTG GTAGCTCACC CTGTAATCCC 1200
AGCACTTTGG GGGACTGAGG CGGGCAGATC ACTTGAGGTC AGGAGTTTGA GACCAGCCTG 1260
GCCAACATGG TGAAACCCGT CTCTACTAAA AATACGAAAA TTAGCTGGGT GTGGTGGTGC 1320
AGACCTGTAG TCCCAGCTTC TCAGGAGGTT GAGGCAGGGG AATCACTTGA ACCTGGGAGG 1380
|
