| Tag | Content |
|---|
EnhancerAtlas ID | HS133-12239 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:8393870-8395080 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr17:8394434-8394449 | TGCCCTTTGACCCTC | - | 6.6 | | Nr2f6 | MA0677.1 | chr17:8394434-8394448 | TGCCCTTTGACCCT | - | 6.43 | | Rxra | MA0512.2 | chr17:8394434-8394448 | TGCCCTTTGACCCT | - | 6.41 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_01584 | chr17:8393512-8395976 | Aorta |
|
| | 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 |
| GH17I008490 | chr17 | 8393581 | 8393960 |
|
Enhancer Sequence | CTAAACCACC GAAGCATCAG GAAAGAGTTG ACCGGGGTGG AGGCACATAT GAAGAACAGC 60
AGTCTTACTG TTTTACAGGC CCACTCGTGG CATGCTGGCC ACTTTGGTCC CCCTGGGCCG 120
GCCCCCTGCC ACATGCATAC ACATCCTTCC CTCTCCCCTG AAAGCTGCTG CTATTCTCCA 180
TTTCAGTGTA TGCAGTTCAG AACTACAGTG CGGATGTCTT TATTCCCACG TGTTCTCTGG 240
TCATCCTCCT CTGATGACCT TTAAGCTGAG AGCTCTTCAG TGAGCCAAAG AACAAAGGAA 300
ACAGCCATGT CAGGGAACCT GTCTGTTGAC TGACTCCTTG CCTGCTGTCT GTGAGGAACA 360
AGTACAACAG TACATCTCTT CTTGCTGTAG AGAAGATCAT TCGTATTGAA AAGCACATGT 420
GGAAACTGCT GATTATTAGG GTGGCTTGGG CCTAAGAAGC AGGGCACAGT ACACAGGCCT 480
TGATCTTTCT CTGGACAAAG ATGCCCCCAG CACCATTTCC CTCATTCTCT GCGCCAAGCA 540
CTGTGCTGAG AGCTCCACCT CCTGTGCCCT TTGACCCTCA CAGCAGCCTT TGGAGGGAGG 600
CCTTGGTGCT GCTGTGCACC CCCTCTGGGG TCCAGGACCA CTGCAGTTCT CACGGGGACA 660
GGCGCGGGGA ATCCTAGGAC AGGAGGAAGG TCCATTTCTA CAGTGTCTGG TGCTCAGTAG 720
GCACAAAAGA CCTGTTTGTG GGATCAACAT GTGAGTGTTG ATGCTACAGA AAACGAACAT 780
GAAATCAACT GTAGAGTTCT CTCTCCACAT TTCACTGTGT AACCATGGCC ACTTCTACTT 840
TCAGTGGCCT CTTTTTGTCC ATGGGGCTAG TCCCTGGGCG CCAAGTTGTA GGAGACCCAG 900
CAGAAAGGTG GGACCACCTT CGCTGACTTA TGATGTGGCC AGATGGCCCA TAGCACATGA 960
AAATGAGATC CTGCCTTTTT AGAGGACTTT GTGTGCTTTT CAAAGCAGAT GCAGTAACTT 1020
CATGAAATTG GGCAAGTATA ATGTCCATCT GGCAGATAAG GAAACTTAGG CTTCAAAAGC 1080
TTAAGTGGCT TCCCATGGTC AGAATGGAAG CCTGTGGAGG AGCCAGGGAA CCTTGCCTTT 1140
GATACCAGGC CTGGGTTTGT TTTGCTATCT TCAACACGTC ATACACTAAG GGAGAGACGT 1200
AGGGTAAATA 1210
|
