| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01574 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:45466060-45467500 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr1:45466739-45466751 | GAGCACGTGGCC | - | 6.92 | | NKX2-5 | MA0063.2 | chr1:45467451-45467461 | CTCAAGTGGT | - | 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 |
| GH01I045001 | chr1 | 45466673 | 45467272 |
|
Enhancer Sequence | CAACCTGGGC GACAGACACG CTGTATAAAT AATAATAATA ATAATGGTTA AAATGAGTGC 60
CCCCTTGGCC CAGTCGTCAT CATTTCCTGC TTTGATTAAT CCCTGCCACC TGTATCCTTC 120
TCAACCCATT CTCTACACAG CCACCAAGGC AAATATAGTT ATGTCACTTT CTTGCTTAAT 180
GCCCTCAGGG CTGCTCATTA TAAAATCCTA AAACTGGCCT TATAAGACTG GAGTCTCATT 240
TCTCTCTTTC TTTTACACTC CAGCAACACA GTACTCAACA GTCTTCTCAG CTGGCCTCTG 300
TGTTGAGTTA CATGCCTTAG GAATTTCGCA TTTCATTGAG CTGCATTGGT TAGAACGATC 360
CTGTTCTGTC CCCTAACAAT TTTCACTTCT TTGTAGCTTT TACAAAAGTG TTCTTAAGTG 420
TTGTTTATGC AACTCTTTGT TTGTATGTCT TTCCCATTAG AGTTTAAATC CCATAAGGGT 480
AAAAATTATC ACTGCTTTAG CCACGATTTT ATCCATTCAC CTAGTGCAGT GCCTGACCTA 540
GGGGCTTGAT GCATATTAGT TTATTGAATG AATGAAGGGT TAAATGAAAT GCAGGCTACA 600
AAATATACAG TGTGAGTAAA AAAGGGACTA AAGAGTTCAT GTGACCATAC CAGGCACAGA 660
AACTGGCTAC TTCCTGTAGG AGCACGTGGC CTGGGCCCTT TCCTGAGGGG AGAGAAGGGA 720
GAGGTGCACC CTGACTTGGG AAGAGCAGAG CTGGGTGGAA GTGGTGGCCT TGGGGGTTTC 780
TGTGCCTTCT GCTTCCTGGA AGGGAAGGGG GTTCACCACC CAAGGTGCAG GGGTACAGGG 840
GAGGCGGTGG CAGCCGAGAG ACTGAGCTGT CAAGTTCCGT GTTTTGGGAT AGGTCTCAGG 900
GTGCACACAG TGCAGGCAGA GATCAACCTC TTGCACAGTA AGTTTCCCAA CTAGGGCAGT 960
GTCAGGGAGT GCCCTAGAGG ACAAGAAGGG GAAGAGTTGC CAGGGCGAGA CTCCGCCAAG 1020
CCACTTATCT GGACAATCAG CCACCACAAG GTCTCACATT GTACCTGGAC TCTGAGACGA 1080
CTGGGACCCT GGGGCTGTGC TTGAGAGCGT GACTGGCCAC TGTGGGGGTG TAGGGGGACT 1140
GTTCGTACAC AGGGTTCTCC CTGATACTCC TTTTTTTTTT TTTGGATAGA GGGTCTCACT 1200
CTGTTGCCCA GGCTGAAGTG CAGTGGCATG ATCTTGGCTC ACTACAACCT CCACCTCCTA 1260
GGCTCAAGCG ATCCTCCCAC CTCAGTCTCC CAACTGGCAC CACAGACACG CACCCAAGCC 1320
CTGCTCATTT TCGTATTTTT AATAGAGAGA GGGTTTCACC ACGTTGGCCA GGCTGGTCTC 1380
CAACTCCTGG GCTCAAGTGG TCCGCCCACC TCAGCCTCCC AAAGTGCTGG AATTCCAGGT 1440
|
