Tag | Content |
---|
EnhancerAtlas ID | HS133-20667 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr21:44447050-44448810 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 44447204 | 44447440 | chr21 | 44447803 | 44447853 |
| | Number: 1 | ID | Chromosome | Start | End |
GH21I043028 | chr21 | 44448119 | 44448190 |
| Enhancer Sequence | TTTTAAATCT TGGACTTTTA AAATTAAGCA ACCTTAGAGC TGATCCAGTT CTAGTGTTGT 60 TGTTTTGCAG AGGGGGGCAT TAAAAAAAGA AAGAAGTTGT CACAGTGACA AACCAGAGTA 120 GAATCTGAGT CTAAAAGTAA TGCTTTTGTT TCCCTGATAT CGTGAACATG GCTACTCAGC 180 TATCCAGATA GAGAAGTCTG GCTTTTAATA GATGAGCAAT GTGTGACTCT AGCAAGAGGT 240 CAACTACTTT ATCATTCATG TTACTGAAAA AAGAAGACAG AAACGAGGCC TTAAGCATGG 300 TTGGTATTGC TGCTTTTGCG TTAGGTTGGG GTAATGCATG AATCTGGACG GGTTCTGGTT 360 TGATAGGCGC TTTCACGGGA CAGATGTTGT TTTTCTTTCC GTTTCTTTCC ATTTCAGCTC 420 TTTTTGTAGC AAAGTGGCCC AGTCAGTGGC ATAGGGTGGT GGGTGCAGCA GAACGCATGT 480 CTGGTTTGCT ATCTTTGTCC TCTAGTCACT GCAGGAGGAA AAGCTGGCCT AGGGATTTGA 540 GTCTCCTTGC ACTTTCTCAC ATTTAAAGGC AACAGCTCAT AGCATAAGAA TGGGAACTGA 600 AGACAGCAGC CTTTAATCTT AATGTATTTT GAGATTGCTA TCATACTCAT TTGATATGAA 660 ACAATGTCCA GCCTGCCTTG CCAACCTGTG ACTGTTGGGC CAGGTGCAGT GGCTCACATC 720 TGTAATCCCA GCACTTTCGG AGACCAAGGC AGGCAGATCA CAAGGTGAAG AGATCGAGAC 780 CATCTTGGCC AACATGGTGT AACCCCGTTT ACTAAAAATA CAAAAATGAG CTGGGCGAGG 840 TGGTGGGCGC CTATAGTCCC ACCTACTCAG GAGGCTGAGG CAGCAGAATC GCTTAAACCC 900 AGGAGGCGGA GGTTGCGGTG AGCTGAGATC GTGCCACTGC ACTCCAGCCT GTGCGACAGG 960 GCGAGACTCC ATCTCAAAAA TACAGAAACA ATGTCCAGCC TGCCCTGCCA GCCTGTGATT 1020 GTTGCTGCTC TCGTTCTCTG TGGAGTCTTA TCACAGGCGT GAGTGCCTGG TCTGACAGAG 1080 TCGCCAGCGT CTGTCGGGGA TTTCATCACT GCTGGTGCCT ACGTGCTGTG CTGGCCACAT 1140 GTCTAGGACC ACTGGAGGAC TTACGCCTCC AGTCATCTAA GAAACAGCTC ATCATTGGGA 1200 ATGGTTTTTG AAAAGATGCA GCTCTTGCCT TAGATCGTGC TTTGTGGTGA AACAAGAGGA 1260 GGTGGCAGTC CCATTCTCTG ATGGCTCAGA CACGTTGCCA CCCAGAGGCT CGGCCCCGTT 1320 GGTGATCTGG TGACGTCCAG ACGAGTGCAG ACTGCCCGAT CGTCTCAGGC ATGATGGCAC 1380 TACAGAAAGT CTTGCTTCTT TAACATTTTT CTTCCTTAGG GAAAACAGTG TCAGATTCAC 1440 AAATTCAACA GTATCATCTA TGTCGTTATG AGTATCTAGT TCACAAACAT GCCCTAAAGG 1500 AGTTGAGACA AAAAAAAAAA TGCCATGGAC GAGTTGGTGC TTATTTGCAT GATTTTTAAA 1560 ACAACAGGCT CTGTGTTTCT GGGCATTTAG AGAATTCAGA AGAGCTGTTG AGTCCTCTTA 1620 AGTAGTTACT ATAGTGGAGA ACTTGAGTCA TTCTTTGTAG CGTGCTTCGT AGAGCAGCGT 1680 GTTTGTTAGA AGGATTTGTT AATCCTGTAT AGGGTCTTTA CGAAGGCTGT TTTCATGGAA 1740 GCTTCTCTTT GTTGACTCCA 1760
|
| |
|
|
|