| Tag | Content |
|---|
EnhancerAtlas ID | HS133-08024 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:110586390-110588250 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr12:110587894-110587906 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr12:110586498-110586513 | TGAACTCCTGACCTC | - | 6.22 | | SOX10 | MA0442.2 | chr12:110586661-110586672 | TGCTTTGTTTT | - | 6.02 | | Sox6 | MA0515.1 | chr12:110588195-110588205 | CCATTGTTTT | + | 6.02 | | TBP | MA0108.2 | chr12:110587666-110587681 | CGGGGGTTTTTATAG | - | 6.84 |
|
| | 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 |
| GH12I110149 | chr12 | 110586806 | 110587205 |
|
Enhancer Sequence | TGCTTCATCC TCCTGAGTAG CTGGGATTAC AGGTGCCCAC CACCATGCCT GGCTAATTTT 60
TGTATATTTA GTAGAGACAG GGTTTCACCA TCTTGGCCAG GCTGGTCTTG AACTCCTGAC 120
CTCATGATCC ACCCGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGTGTG AGCCACCGTG 180
CCTGGCCCTG GACTACTTTT ATAAAGAGAA AACCTCTCAT CAACTATTTG GTTATCCTGA 240
GTTATAGTTC ATATAGGATA GGCAGGGTAC ATGCTTTGTT TTTATCATTA TTTATCAGTT 300
TTCATAATGA ATTTGTTTCC TCTAACTCAT TTGCATCCTC CAACAGTGAA GTGATCAATT 360
AGGGCTATTT TTTGTTGTTT TTTGTTTATT TAATCTCATT ATGAATCCTA GACATTATAA 420
GTTTTAAACA GTATCCTTAA TGATGCTCAA ATTGTCCCAG TTTTGGCTAA TGGGAGGCTT 480
TTCAAGTTAA CTTTTGACTT CTTTTCAGAT TCTAGTGGTC TTTGATAATT TCCTTGCTTT 540
CTGCATTATT TAAGTCATTT CTAGGCTCAT CGTTTACATT TCCTACTCTA GACCTGGAAT 600
TAGGCTTTCT TCTATGAACC TGGTTTGTTT TAGCAGGAAA TGGTATTTAG AAACTGAAAC 660
AGGGAAAGTT CCCTTGTCCC CATCGCAGGG CATGTGACAG GGGGAGTGGC TCGCTTCTTT 720
AGTGCCCCAC TGCTCAAACC TCTAGAGGAG GTATAGACAG GCAGGTTGTG GGGCTCTGTC 780
CCCACAGCAG TGTCTAAGGG TGAATGTTTA CAGCGGAAGC CCCAGTGGGC ATGTGTTACA 840
GTGTGCTCTT TTAGTTTAGC CATCCATAGG CGGCTTGTGT TAGTCAGCTC AATTAGACCC 900
CTACCTTATC ACAAGGACAG AGGGCTTTCT GTATCCCTGG GGTTCTTGTC TTGGTGTACC 960
GGAAGAACGG ATCACATGTG CTCTTGGAGA ATGGGTGTAA GGTTTTATGG AAGTAGCTTT 1020
CAGCAGATAG GGGAGCCCGA AGGGAGATGG TTTTCCCTTG GAGTCAGGCC GCCGAGTGGC 1080
CTGACTCTTC TTTGACCACC CTGACTCTTC TCCCACTGCC CCATCCTAAC TCTGCGTCGT 1140
TCTGCCAGTC AATGGCCTAG GTCAGTCAGT GGCCTGCCAG TGCCTGTCGG TGTCTCTAGG 1200
TATCAAGCCA CTTGTGTCTT CTTCAGCCGA TCTCCTCTTG ATGTCCGGCC ACTTGTGTGT 1260
CTGCCTGCTA GGGTCCCGGG GGTTTTTATA GGCACAGGAT GGGGGCATGG CAGACCAGGG 1320
TGGTCTCGGG AAATGCAACA TTTGGGCATG AAGGCAGGAG TGCCTGTCCT CACCTAGGTC 1380
CATGGGGACA GACCTGGGGG TGGAGCCCTC ACCAGGGACC ATGCCCTCCT CTACCCAGCA 1440
CTTCCCTGCC CCACTTCTGT ATCAAAACCA CAGTCTGGGT GTTAGGAGTT CTCGTTGATT 1500
TTTTGTTTGT TTGTTTTCTT TTCTTTTCTT TTTTTTTTTG AGACAGAGTC TCGCTTTGTC 1560
ACCCAGCCGG GAGTGCAATG GCATGATCTT GGCTCACTAC AACCTCCGCC TCCTGGGTTC 1620
AAGCGATTCT CCTGCCTCAG CTTCCCAAGT AGCTGGGATT ACAGGCACAT TCCACCACGT 1680
CCGGCTCATT TTGTATTTTT AGTAGAGACA GGGTTTCACC ATGTTGGTCA GGCTGGTCTT 1740
GAACTCCTCC CAAAGTGCTG GAATTACAGG TGTGAGCCAC CGCACCCGGC CATGTTTTTA 1800
GGCAGCCATT GTTTTTAGGT CTTTTCAGTG GACCAGGCTA GGAGGTATTT CTTTCTCTTT 1860
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