| Tag | Content |
|---|
EnhancerAtlas ID | HS133-05722 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:61872320-61873680 |
Target genes | | Number: 28 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr11:61872339-61872351 | AAACAAACAAAC | - | 6.32 | | MEF2C | MA0497.1 | chr11:61873527-61873542 | TTTTATTTTTAGTAC | - | 6.09 | | SRF | MA0083.3 | chr11:61872758-61872774 | TTACCCTATATGGTCT | + | 6.07 | | STAT1 | MA0137.3 | chr11:61872815-61872826 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr11:61872812-61872826 | CCTTTTCCTGGAAA | - | 6.91 |
|
| | 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 |
| GH11I062104 | chr11 | 61871666 | 61874160 |
|
Enhancer Sequence | GAGGGAGACT CCATCTCAAA AACAAACAAA CAAAAACCAC CAGCAACAAC AACAACAAAA 60
CACCTCTTTC CTTTATATAA GTTACCCAGT CTCAGGTATT TCTTCATAGC AGTGTGGGAA 120
TGAACTAATA CAGGTGACTA CTCACATGTG GCAAATGCAG ACAAGGGCAC TCTGTGCTAT 180
TGGGATGCTG AGGTGGGGGT GTGATAGGAG TTTGGCAGGA CTTGTTTCCC AAGACATAGG 240
TCACAAGGAC CCCCCTGATA AAACAGGATG TGGTAAAGGA GCCAGCCAAA ACCCCCCAAA 300
ACCAAGATGG TGATGAAAGC GACCCTTGGT CCTCTCACCG CTCATTATAC ACTAATCATA 360
ATCCATGATT TGTCCATGGT GAAGGAAACT CCCACCAGAA ACACGACAGC TTACATACGC 420
CATGGCAACA TCCGGAAGTT ACCCTATATG GTCTAAAAAG GGGAGGAACT CTCATTTCTG 480
GGAATTCTCT GACCTTTTCC TGGAAAATTC ATGAATAAGC CACCCTTGTT TAGCATGTGA 540
GCAAGAAACA AACATAAAAA TAGCAACCTG CAACTCTCAC GGCTGCTCTT CCGATGGCAT 600
AGCCACTCTT ACTCCTTTAC TTTTAAAATA AACTTGCTTT CACTTTACTC TGTTAACTCT 660
TGAATTCCTT CCTGTGCAAA GCCAAGAACT CACGTCGCCT CCTGGGCTGA ACTCCAATGT 720
GGGGGTTCAC CCTGTGACAG GTGGATGGGC TGGAGTCCAG GAGTTCGGGT CCAGCCTAAG 780
CAACATAGTG AGACCCCCCA TCTCTATTTT TTTCTCAGAC AGTATAAGAG ACAGATGAAG 840
CAAAGTGCAT AAATGGCTGT GAGGAGCATG TGGTTTGTCA AAGCTGGAAC TTTATTTACA 900
AACAAGTTCC AGCATTATCT GAGTGGGTGC TGCTAACAAT TATAGCGTGT TCTTTCAAAC 960
TGCAGACTGG GATTAGACGG TTTGCCAAAA AGCCACTGAG TACATCAAAG CGAGAATTCT 1020
GAATTCTCCA TTTATCTTCA GATTTATCAC TCCCTCCCTC TGTGCCCTTC TCTGCATCTG 1080
CTGTATGTGA GTATGGAGAG TCCACACAAT TCAGTCTGTA CCAGTGGTCT AGGTTTTCAA 1140
CTACATCTCA TTGGTCAAGC ATGTTTGCAT TCACAGAAGG AACCCTACCC CCATTTTTGT 1200
TTTCCTGTTT TATTTTTAGT ACATTTTAGG CCTTAAGAAT GTAGGGTTTT TTTGTTTGTT 1260
TTTTTTTCCT ATGAGACGGG AGTCTTGCTC CATAACCCAG GCTGGAATGC AGTGGCATGA 1320
TCTCGGCTCA CTGCAACCTC CCCGTCCCGG GTTCAAGCGA 1360
|
