| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00172 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:6426810-6429090 |
Target genes | | Number: 23 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:6427804-6427822 | TCTTCTTTCCTTCCCTTC | - | 6.04 |
|
| | 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 |
| GH01I006367 | chr1 | 6427174 | 6429080 |
|
Enhancer Sequence | GTTCAAGTGA TTCCCCTGGC TCAGCCTCCT GAGTAGCTGG GACTACAGGT GTGCACCACC 60
ACACCAGGCT AATTTTTTGT ATTTTAGTAG AGATGGGGAG AACATGTCAG CCAAGATGGT 120
CTCGATCTCC TAGACCAGCC CAGTAGAACT TTCAAAAGTG GAGTCAGGCC GGGCGCGGTG 180
GCTCATGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA GGCGGATCAC GAGGTCAGGA 240
GATGGAGACC ATGATGGCTA ACATGGTGAA ACCCCTTCTC TACTAAAAAT ATAAAAAAAT 300
TAGCTGGGCA TGGTGGCAGG CACCTGTAGT CCCAGCTACT CGGGAGGCTG AGGCAAGAGA 360
ATTGCGTGAA CCCAGAAGGC AGAGCTTGCA GTGAGCTGAG ATCGCACCAC TGCACTCCAG 420
CCTGGGCGAC AGAGCGAGAC TCCATTTCAA AAAAAAAAAA AAAAGTGGAG TCAGTCCTCT 480
TAAAACCTAT GTTGTTTTAT CAACTAAGTT TATGGAATAT TCTAAATCCT TTTGTTATGG 540
GATCTTTGGG GTATCCCTTT TCTGGCCAGA AACCTCTGTG TCTTGTGGCA CCTTTGCCTA 600
AGTTTTGCTG GGGCCCACTG GGCTTATTCC ACCCACTCAG CCTGGCAGGC TGCGCTTGGC 660
TCATGCTACC AGCCTGGAGC TCCCATGCCT GCCAAGGACA AGCCTGGTGT GGAGCAGCGA 720
GCAGTGTGTG AGTGAGCATG GAGTACGGCC ACTGCACAGT CAGACATGCC AGCTGCTGCT 780
GCAGGGCAGG CAGCTCCAGA TGCTGGCACA GGTGCTGGTT CTCTGCAAGG CTGCACCTGG 840
ACCAAGCGCA CCTCAAGCAG CTTGCCTGGT TGGCACACGG GAATGCTGTG GTGCCTGGAA 900
GCTTGGTGAC GCCAGGAACT GCAGGGCCCC AAAGAGGGAG TCACAACCCT GACTCAGGGA 960
GCTCCCAGGT CTGGACTCCC CAAAGGGCCA CAGCTCTTCT TTCCTTCCCT TCACTGGCAA 1020
CGTGGCAAGA AGGGGCATGT TTCAGCCCTG TTTGTGTTAC AGTTCTTTCA GCCTCACCAT 1080
TTGGCAGGTC CCGAGTTCTT GCCCTGTGAC CAGGAAGAAT GAGGTACGCA GAAAAATGGA 1140
GAGTGAGCAA GACAAAGAGG AGCTTTATTG AGTCACAGCC AGGTCATCCC AGTGAGTGTT 1200
CAGCTCTCAG CAGAGAGGGT AGCTCTTCTT TGCAGCTGGT CATCCTGTCA TCTTTCTGTC 1260
CTCTGCTCTA GTCTGGCTGA GTCCGGGGTT TTTATGGGCC TCAGAGTGGA GGAAGTGTGT 1320
GTTGACTGGT CCATGGGTGG GCCAGCAAAA AGCACCACAA GCTTCCCCTC TGGTCCTCGG 1380
GACTGGCCAG CCAACCCCCA GGCTTCAGGC CCTCCCCAGT TTGAAGGTGA GGCTTCACTG 1440
GGGACCAGAC CCCTTCTACC CAGGAGCCTG TCTGTCTCTC GCCACTGTTC ATGGCATCCA 1500
GGCTGTTTGT GCCAGCCTAT CCTCAGCCCC CACTTGGCCT CCCTCCCATG CCTGTTGGTG 1560
CCCAAAGTCT GAAGGGCACC ATCAGCAGGG TGGGTGCGGT GGCTGCACCG CAGTCCAGGT 1620
CCCCAAAGTG AATGCCGCTC CCACTTCCCG CCCCAGGGCC CTGAAGCATA ACCCAAGCTC 1680
TGCATCCCAG GCCCAGCCCC CACACTCCAT ATGCAGGTGC AGCATCACCC CAGGCCCAGC 1740
TCCACCTTGG GGCCCCTCTC TGCCCGCACC TCCATGCCCA ATCATGCTGC TTCCCCACCA 1800
GCAGGCAACT CAGCCTGGCC CCGTTGTGGT GGCTCCCAGG GCAGTGGGCT CTGGGAGACT 1860
CCCAGGGGTA GACTCCAGGG ACTGACTATT TCCTCTGCAC ACCCCTCCCC ACAGTGAGAG 1920
CGGGTAAGAG CTCTGACACT GAGCCAGGGT CTGGAGCGGC AAGGCTCCAG GCCTGGGAGC 1980
AGGTCCTGCC TGGCTGTGCA AGGATGGGGG CGGTGCAGTC AGCTGCCCGG GGAATGCAGG 2040
GCACAGGGGA CCCACTGCTG CCACTGCTGC TGCCACTGCT GCTCCCACAG CTGCTCCTGC 2100
CACCACTGCT TGCACCACCC CACTGCACCT GGCGTGAGGG CAGGGGTTGC TCCAGATGGC 2160
CCACCATTGC CATTACTTTC TTGTCATTTC AGCAATGTTC ATGGCATCTT CCCCAAGACT 2220
ACATTCCATC TTAAGAAACC ACTTTCTTTT TTTTTCTTTT TTGCTCTGTT GCCCAGGCTG 2280
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