| Tag | Content |
|---|
EnhancerAtlas ID | HS002-08374 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr6:53727180-53728580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:53728041-53728059 | CCTCCCTGCCCTCCTCCC | - | 6.27 | | EWSR1-FLI1 | MA0149.1 | chr6:53728037-53728055 | CCTTCCTCCCTGCCCTCC | - | 6.89 | | ZNF263 | MA0528.1 | chr6:53728040-53728061 | TCCTCCCTGCCCTCCTCCCTT | - | 6.15 | | ZNF263 | MA0528.1 | chr6:53728037-53728058 | CCTTCCTCCCTGCCCTCCTCC | - | 8.44 |
|
| | 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 |
| GH06I053861 | chr6 | 53726202 | 53729926 |
|
Enhancer Sequence | ATTTTTTTCT GCACATTATC CCATATGAAA CCTCACATTT AATATTCTGG AATTCACCTT 60
TACTTTGTGT GTGTGTGAAT CAGCATCTTG TACCCCAGGA CATGTTTGTG TTTATTTAAG 120
CCAACTCCGT GTGGGAGGAA AAGCTGAGGT ATAAGGGTTA TTTTGGTAAT TGTGGCTTTA 180
GGTGAAAACC TTTTTGATTA GGAAAAATTT CTGCCAGCGC AAGTACCAAG AATTGTGCAA 240
AATAAAATTT TACAAAGGCC GTCTCTCTTT CCTGCCTCCC CTTCTGTACC ATCAGGAGAC 300
CCATGCCGCT CAGCCTGTGT ATGCTCTGGA AAGGCTGCTT GGAATTATGG CTTTGTCTAC 360
AAGGCTGGCT GCCTCCTCAG TGAGTCTGTG GTGGTTGGAA TAATATGATA AATGGGATGC 420
ATTTGAAAAA AATTCTCCAT TTAACATTTT TTTCCCCCTG CACACCCGGA ACAACAGCTG 480
TGGTAGCAAA TGCAGACTTG GCTCATGGAT TCATATTTAG TCTTGTTTGA CAATTCCAGA 540
TATTTTTAAG CAGGATTGAG TCAGGCAGCC CACAGCACGG CATTCAAACT GTCTTAATCA 600
GCCAGCCTGT TTGGCACACA AGGACTTTGT TTTATCCTAG TAGTAAATAA TTCTAAATCA 660
AGCAATATGA TGTACTGAAT GTACCCAAAG TCACAGCATT CAGTATTTTA CTACAGCCTG 720
TCAGCATCTC TTTTTACATG CTTGTTCTGT TCACTGCTAG TTGTTTTATT CATTATAGCT 780
TTTGAATTCC ATTCTTGGCC AGGTCTGGAT TCATGGTTTT CATACATAAT AGGATCCTAT 840
GTTTTCTGCC CTGTGGCCCT TCCTCCCTGC CCTCCTCCCT TTACATAGCA TTGCCAAGTA 900
GATGCAGTGT TCATTTTTGC CCAGAAGGGT TTCCTATTGT GACACCTCAT TTCCTTCTTA 960
GGATCATGGG ATTTTGTCGT TTGCCTCTTC TGTGGATGAG TGAATCTCAT CCCAAGAGCC 1020
TGTTTTCGAT GTATGGGGTT TCTTACACTG TTCCAGGTCT TCCGCTCCCG GGCTCTTCTT 1080
CATCTCTCCA CGTAGATAGG TCTCTGAAGT CTTTATGTTC AAGCCCTCCC TTCAGCTCTG 1140
TGGCTGTCCT TGCTGCCTTC TGAAGAAGGA CTTTGTTTGT CTTGTCTACC TCTCTGCTAG 1200
CTCCTCAGAT TTTCCAGATA AGTCAAACCC GAAAACATCA GAATGAACTT TCCCTTGACC 1260
TTGGTATTCT CCTCAAGCTA TTCACCCTTT TTCTCTTCTG GTTGCCAGGC TTTTTGAAGG 1320
TATACTCTAC CCCATGTTCT CAGATGTGGA GATTTAACAG AACAGTGTAA TTTTTTTAAT 1380
GGGATCTGAC ACAGGATTGC 1400
|
