| Tag | Content |
|---|
EnhancerAtlas ID | HS098-34608 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr20:34579200-34581020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr20:34580825-34580844 | TTACCACTAGAGGGCAAAA | + | 6.4 | | SREBF2 | MA0596.1 | chr20:34579659-34579669 | ATCACCCCAT | - | 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 |
| GH20I035992 | chr20 | 34580741 | 34580910 |
|
Enhancer Sequence | TTATTTATAA ATTGTGTGTA ACACATTCTG TATAACAGGT TTATATGCAG GCATATGTTT 60
TTTAGGAGAG CTGGTTGTTA AACTTACCAG CACCACCAGG GGCGTGGTGT GTGTGTTGTT 120
ATTCTCGGCT CAGTCCCAGA GAACAGAATC AAGTCTAGTT AATATAAGTA GCAAAAGATT 180
TATTGCCAGA TATCAATTGG CAGTTCCTTC TCCTCCTTGA TATTTGCTTC CTCTGTGCTA 240
AAATTTTGAG GTGATCACCT CTGCCATATC TCTCCAAATT TAACTCTAAG CTCTTTGATA 300
CTATATAGCC AGAAAAGATG GGGGGATGTG TGGTGAGGGA TAGAAATCCT TTACAATATT 360
TTCTTTAATC AGCATAATGA TTACATTCTG ACTGGCAGAA AGCGGGGGGT GGTTCTTCAT 420
CTGTTTTGCC TCCATTGCTT CACCTGTGAA ATGGTACCAA TCACCCCATA AAGTCTGGTA 480
AGGATGAGAA TCAGTTTAGT ACATGCTTAC TCAGTGAGCA TTCCTCCCGC AATCCAGTGC 540
TTCTCAAAGT GCGGTGGCTG GACCAGCAGC ACCAGCAGCA CTTGGGAACT CATTTCTTCT 600
TCTTTTATTT TTTTTTTTTG AGATGGAGTT TCATTCCTGT CGCCCAGGCT GGAGTGCAAT 660
GGCACGATCT TGGCTCACTG CAACCTCCAC CTCCTGGGTT CAAGTGATTC TCCTGCCTCA 720
GCCTCCTGAG TAGCTGGGAT TACAGGTGCC CGCCACCAGG CCTGGCTAAT TTTTGTATTT 780
TTAGTAGAGA TGGGATTTCA CCATGTTGGC CAGGCTGGTC TCAAACTCCT GACCTCAGGT 840
GTTCCACCCT CCTCGGCCTC CCAAAGTGCT GGGATTACAG GCATGAACCA CCGCGCCTGG 900
CGGGGAACTC ATTTCAAAAT GCAAATTCTC AGGCCCACCC AAGAGCTACT CAATCCAAAA 960
CTCTAGGAGG AAGGGCTCAG TGATCTGTGT TTTAACAAGG CTTCCAGGCG ATTCCAATGC 1020
ACACTGATGT AGGAGAACCC CTGACCTAAG GGAGGAATTT TCAAATTTTG GTAAGCATCC 1080
AGACATGTAG GGTGCTTCCT GAGGGAGGAA TTCTCAAACT TTGGTAAGCA TACAAACACA 1140
TAGGGTGCTT TTTAAAAAGG CAGATTTGCT GTCTCACCCC AGAGATTGAT TCATTAACTC 1200
TGGAATCTGC ATTTGAGCAA GTGCTGTAGG GGATTCTAAT GCAGGGGTGC TGAGCCTTCA 1260
TTCTGAGAAA AATAATGCGG AAGTCACTAA AGGACAGCAA GGTAGGGAGC TCTTGGCCAG 1320
AAGATGAATC TGGTTTGTTC CTTACAGTGT TTTATTAAAA TCTGATTTAA TCATCAATGT 1380
GAAGATTTTA TATAAAAATT CTGATTTCTG GCTTTTGAGA ATTCAGAGGA TCAGGCAACA 1440
ACAAGCCATA TTTTGGTACA GCACCCCCTC CCCCACCCCC CGACCCTGGT TGGAAATGAA 1500
AAGCACCAGC CCCCTCTAAA GGACTGCTCT TTTCTCTCTT TTTTTTTCCT GCCTGGCCAG 1560
CGTTTTTTGA GTGTTCATCT CTGGGAGGGA GATCAAGCTG TCCCGACTCC TGTAGTTTAC 1620
TCATATTACC ACTAGAGGGC AAAATCAGCT GCGGGTGGCT GGACACCCCT GGGACCTCAG 1680
AAAGCTAGAG AAGATTTCCT GATGGCATCG AAAACTTAAT GCACACTTTC AACTCATTTC 1740
TAACAGTTTA TCACTGGGGG ACACATAGTG GAACTGTTCT CTCCATAGAT GCAATTAAAG 1800
ACCTACTAAA TACTTGAGGA 1820
|
