| Tag | Content |
|---|
EnhancerAtlas ID | HS133-13519 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:76665230-76667670 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCFL5 | MA0632.2 | chr17:76666379-76666389 | TCACGCGCAC | + | 6.02 | | ZNF263 | MA0528.1 | chr17:76666140-76666161 | CCCCTCGCTCCCTGCTCCTCC | - | 6.63 | | Zfx | MA0146.2 | chr17:76666968-76666982 | GCGGGCCAGGCCTG | + | 6.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 76665989 | 76666227 | | chr17 | 76666953 | 76667003 |
|
Enhancer Sequence | CCCAGGCCCA ACACTTAGGA CTCATCCTGA TTTCTCCTTC TCCCTCCATT TCTACCTCCA 60
AGTTCTGCTG CCCCTCCCTC GAAGGCACAT CATGAATTTT TAATTGTCCC CTACACCTCT 120
CTCACGGTTG TCCCAGTACA ATCCCCATCA CCCCCAACTG AGTCATGTCA CAGCCTCGTG 180
CTGGCACTGT CCTCCCCCAA CAATTCTCCC TCCAGCAGCC AGAGTCCCTC TCCAGCCCCC 240
AAGCTCCACG CCACCTCAGA CGTCCCCTAC CATGGCCCTG GTCCCGCTCC ATCTGGCCCC 300
TGCTGACCTC TCCTCTGCAT CCCCTGCCAC CCCAGGCCTT AGCCAGCCCA TCCCAGCAAT 360
TCCTTCAGGA TCCCTCCACC CCACCACTAG CTACCCTACT CTAAGCGGCG CCCCGGGCCC 420
TTGCCTGGTG GCCTCCTCTT CAGCTCAGCA ACCTCTTCTC AGTGGGGCCT TCCCTCATCA 480
GCCCGTTCAA GTTACCTCCT CCGCTTGCTC TTTCCAATAG CCGCCCACCT GTTTGCTCCT 540
GGGGTTAGCC CCCCACACCC CGGGATCACT TCACTCAATT TTCTCATGTC TGCTCTACCC 600
AGACTCTGAG CGCCAGACAC GGGTTCTCAC TGCTCCCAGT CTCCACCTTT GGCGGCCACA 660
GCCTTTCTGC CGACCTAGCA TCCATTCTCC ACCCTCTGCT TGCCGGCGTC CGGCCCACGG 720
TACCCCAACT GTGTCTGCAG GATGTGTGCC CAGCCCCAGT GAGGCATCAA ATGGGCCTAA 780
GCGGAGGATT GGCTGAGAGG TGGAGACGAG ACCCAGGGTG ATGCTGAAAC GTAAGGACAC 840
GTCTGCAGGG AATCCGGGGA AAGACACTTC CTCCTTGATG AAGGGAGGCA AGCATGGGGG 900
GCCCTGGCTG CCCCTCGCTC CCTGCTCCTC CTTCTGAGTG CCACTGTGTG AGGATATGGT 960
ATCCCCTCCT TCTAACTGTG CCACGACCGG GTCAATATGA GTGTTCCAGG AGAGCGGAGG 1020
AGGAGGAAAG CTCCGGGTTA CATCCCAGGG CAGCCGAACA ACCTGGAGCG CACATTTGGG 1080
ACTTCCTGTT CTTATTTGTG TCCTCATGAG TCATGTCCCC ACTAGGTGAG CTCTCTGTGA 1140
CGTGCAGCCT CACGCGCACT GACAGGCATG AAGCCCAGCG CTGGGCGCAT GGGACCTGCT 1200
CCATCAGGTT AGAAGCAGGG AACAAACGCC TCACGGCTCC TGCTCCCAAC ACAACCATGG 1260
AGACAGGCAC GTCCGCATAA GCCATCCCAG AACCGAGTGG ACTCACTGCT CAGGAGCACG 1320
AGGAGGCCCT TCAGCCTGGG GAAAAAGCTG GGCCAATCTG GACGGCGCAA GGCTTCGAAG 1380
AATGAGAAGG TTTTGCACAA ACAGGCTGGC AGAGGAGATG GCAAAAGGAA GTCTCATGAG 1440
CAAAGCTATT AGCTATTAAA CGGTGGCTGT GGAGCAAGAG CTTGGGACAC AGGGCAGGGA 1500
GGGCGCAGTT AAGGATAGAA ACAGCTAGAG ATAAGGCGAA CAGAGCCTGG TGGAGAAGGC 1560
CTTGAGCATC ATGCAGATTC ACGTTCTCTT CTGCAAGCAA AGGGACAGGT TCTGTTTGCT 1620
TGTTTTACTA AATGGAGGAA TGACATGATC AGTAGATGAA AATTCCACAG CCGCATCAAT 1680
CACGGAGTAG AAGATGGCAA AGCCTAGAGG TCCGCAGACC AGTGGGGAAG CCACCCCCGC 1740
GGGCCAGGCC TGTGATGAAG GTCTTGGGGC GGCGACAGTG GCTGGAGGAG CCACTCCAGA 1800
GGTCCACAGG GAGGGCTTGG GAATGCCTGG GTGTAGGGAG AGAGGGGGAG ACACATGAGA 1860
AAGGGCTCCA AGCCTACACA GGCTCTCTGA GGGTGGCAGC AGAGTCCCCA GGACAAGGGG 1920
CAGTCTTGGG GCTATCAGCT GTGGACAGGC TGAGCTGGGG AGGCCCGGCA GCCACTCTGG 1980
TGGAGACGTC CCACAAGCAG TCAGAGGTGG AAAGGGGAGC CTGGAACGGG CCGGAATTGC 2040
ACAGGCACAC ATAGGGGCCC ACAGCGGGTA GCAGCAGGGT CAGTCGCGGG ACTGATTATC 2100
TGTCAAGGAA GAGGGCTTAG GAACACTGGG GGCTAGAATC CTGGGGGATG TCCAGCAGCT 2160
GGCGGGTGGG CAGAGAGGAG AGGCCAGGGA AAGAACGCAC AGGGAGCTGT CAGAGAGGTA 2220
GGAGAGCCCA GGTAGACTAA TCCACCAGAG CCAAGAGGAG AGAGGAGGGG GACCCCTGGC 2280
TGAGGAGTGA ACGAAAGTGA GGACATAGAT GCAACGAGGA ACTGTCGGAG TCCCTGTTAG 2340
CAATGCAAAA TGTTTGTTCC CTGGTGTCAC AAGGAAAAAT TAGCATTCAG ACAAAAAGTT 2400
CTCTCAGCGA GGCAATTTTT ACTTTCTGCA GAAAGGGTGT 2440
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