| Tag | Content |
|---|
EnhancerAtlas ID | HS133-29268 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:101016190-101017920 |
Target genes | | Number: 26 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr7:101017022-101017037 | CTTTTCCTGAGAATC | + | 6.34 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_68974 | chr7:101016134-101016944 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 101016768 | 101016820 | | chr7 | 101016888 | 101017832 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH07I101372 | chr7 | 101016135 | 101016944 | | GH07I101373 | chr7 | 101017201 | 101017350 |
|
Enhancer Sequence | GCTTGAGCCC AGGAGTTTGA GGCCGCAGTG AACTATGATC GTGCCACTGC ACTCCAATCA 60
GGGTGACAGA GCAAGAGCAG ACCATGGGCT TGGGCAGGCA GAGGACAGGC ACTGAGCTTT 120
TGGAGTCTGG ATGTGAAGTC TCCTTCCTGC CACCTTGAGG AGCTTGCCTT CATAGTCTGG 180
GCTTTGTCAC AGTCAGGCTT GTGCCAACTT TGCTGGTCGG GGAGAGGCTG GCAGAGGAAG 240
GATAGTGGAA GGAGGGAGGC CAGTTAGGAG GTAGTTGATG GATGGAGCAG GGGAGAAGGG 300
AGTGCTCAGA GCTAGCAGGA CCTGGCCCCT TGGTGGATCA CGGATAGGCA GAGACAGGCT 360
ACAGGCCTGA GCTCCTGGCT GTCTCCAGTG CCTGGGGGAC ACCAAGGAGC CTGCTGCTTT 420
GCTTCTCAGA ACATTGCAAA TTTTTTGCAG CACTTTCTTG GTTTGCAATG GCAGCAAAGC 480
AGAGTTCAAA CATCTTGCAT TTTTGTGAAA TACTTTTATT TTTCCTGCAT GGAGTTTTCA 540
ACCCCAAATT TCAGCATCTC CTGGACTTGC ACGGATCAGG TGCTCAAGGA AAGTTTGTTG 600
AGTGAATGAA TGAACACATG AATGAATGAA CAAATACCTT GACCTTTCTC CTTTGGGACA 660
CCGAGGCAGT GCCTCTGCCT CAGTGCACGT TTGCAGTTCT GAGGGATCCT GGAGCGAGGT 720
CCCTTTCTCT GCACAGGCCA GCTCCTGAAG CTGCTTTTAG GGGAACCATG GAGACTCCAG 780
CTTTAGAGGT CCCGCTTCTC CCTTTGAAGT GTGAGCACAT AGAGGAGGGA GACTTTTCCT 840
GAGAATCACA CAGAATGGCT TTGATGTTAA TATCAGTGAG ACCTTGTCCT CAAGCTCCAG 900
GATTTTCTGA ATCTTCCCTC TCTTCATCTC ACTCCCCTCT TCCCCCAGCT CATCTGTTAT 960
TTTAAAATCC ATTCCCAGAG AAACAATTCC TATGGCAATA AGAGCACTCC TCCAGGCTTC 1020
TCTTGGCTCG AACTCGTGTG ACACTTCATT GCCACTTCCA GAGTGTGTGA GCTGGACCCG 1080
GACCAATTCA GCCTGGGGCA GGGGAAAAGA GCAACAATAA CTAACTGTTA GAGGATTTTC 1140
GGGAATGTTA GCACAAAGTG CTCCGGGAAT TCTGCAGACA ATCCTACGGA AACATACACA 1200
TGCCGTGCTG TTCTGCCCTC CGAGTTGTCA GGGGTCCCTG GCCTTCCCAG CCTGGCCTTG 1260
TCTCTACCTG CCTCCCAGAA ACCAGGGTCT AGAGCTTCTC TTCGGAGTCC TGTAACAGAC 1320
TACCCTGAAA CAAGCTGGAC TGAGTCCAGG TTAATTCTGA AATACTGGAG GAGAGCGGTG 1380
TGCGTTCTGG CCCCCTGCAT CTCCTTGTTT GCCCCACCCC TAACTACCTC CAGAGTGATC 1440
TATGTAAAGC AGGAGTCCCC AACCCTGAGG TCACAGACAA GTACCGGTTC AAGACCAGTT 1500
CAAGGAACCG GGCCGCACAG CAGGAGGTGA GTGATAGGCG AAAAAGCCTG AAGCTTCATC 1560
TCTACAGCTG CTGCCCTCGC TCGCATTACT GCCTTAGCTC TGCCTCCTGT CAGACCAGCA 1620
GCGGCAGTAG ATTTTCATAG GAGCTCCAGC CCTGTTGTAA ACTGCACAGG CGAGGGATCT 1680
AGGTTATGCA CTTTTATGAG AATCTGATGT CTGATGATCT GTCATTGTCT 1730
|
