| Tag | Content |
|---|
EnhancerAtlas ID | HS133-28041 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:18485090-18486850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GRHL1 | MA0647.1 | chr7:18485526-18485538 | AAAACCGGTTTA | - | 6.44 | | GRHL1 | MA0647.1 | chr7:18485526-18485538 | AAAACCGGTTTA | + | 6.92 | | TFAP2C | MA0524.2 | chr7:18485303-18485315 | TGCCCCGAGGCA | + | 6.14 | | TFCP2 | MA0145.3 | chr7:18485527-18485537 | AAACCGGTTT | + | 6.02 | | TFCP2 | MA0145.3 | chr7:18485527-18485537 | AAACCGGTTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTCAAAATT TAATGCTGAA ATATGTAGGG GCTGAGCGGC CTCTGTGATT GTTTCAGATT 60
GCATCTTCCA TTGTTGAAAG AATTACCTGT GATATCAATT AATGTTCATA GAATTTTCGG 120
AGCCAATTTT AATGAAAAGT TAAACCCAGT ACTGTTTATC AGTGCCAGTA ATTGCTCTCC 180
TGTATGTTAT AACCAGGCCT ATCTATTCCC AAATGCCCCG AGGCAGAGCT GTTTATAGAT 240
AGCCATGAAA ACAATGTTTT GAAACTTCAG CTTGCCTGAA TCAAAAACCT CCTTTTATGC 300
ATGGTTAGTT AAATCAGCCA AAAAGATAGT TGACAGCAAT ATTTGAAAAT ATCCTGAAAA 360
TGGTTTGACC TTTTCATTAG GTGCTAGAAA TAAAAGCAGA GAATTAAAAG AAGACTTCTA 420
TTTAACCTTT TGAACAAAAA CCGGTTTACA AGTCAAACAT ATCTTAGGAT TGTGCGTGAG 480
CTGCTGATGA CATAGACACT CATTTGCTCC TTAAAGAACA AAATTTGAGC ACAAGGAAAG 540
AAAACCTTTC TCTGGAACAA GTAAGCTCTA TTTAAAAAGT GTAGGTCTCT ATTTAAAGAG 600
AGTAGGGCTG GCAAAGGCCT TTGTCGTCTG GCCAGCAAAG AGGATAATGT GCAGAGACAT 660
TTAAATTCAG TGGGACAAAC ACTACCCTTT GTTGGCTCCC ACACTCTCAG ACACACACAC 720
AGAACTTCCA CTAAAGTGAG AGAACTGTAT CTAATTTGGA ATTCAGAAGA TGGCCAAAAA 780
TAAATAGTTT ATTGTCATAT TCAGATATTA TATTCATGGT TTTCTAGGTT GGTGTGTATG 840
ACATCACTGC TTTAAACCCA GCCATGCATC AGCATTGGTC ACTGTTCTTT CTCATGCCTA 900
GTCGGGGGGT GGGTTTAAAA GAAGAAAGTG TTGAGCATAG ATTTGACAGG ACTTGAAAAC 960
TGGGAAAGGT TTAGGGATAC ACTTTTGAGT TGAATCTTTT CCTTTTTGCT AATGCTGCTT 1020
CTCATATAAC GTATATTCAA ATATATTAGG TTTTTTAATT ACAAAAGTAA TACTTGCTTA 1080
TTGTTTTCAA ATATATTATG GGTAAGCTGT TTTTTAAAAA GTGAAACTGT CTTTCTGCCT 1140
CTATGTCCAC ATCCTCAGCA AAAGCACTGT TGATATAGTT TTTTTCAACC TTTTTGCTAT 1200
GCATTTACAA ATATACACGT TCTTTTGTGT GTGCGTAGAT GTAGAACATA TATTCCAAGT 1260
GTCATTGAGA ACAACATATA TTTTCCTGCA AGATGCATTT TTTGAAAAAA ACTTGGAAAT 1320
ATCAAGGGCT GCCTTCTGTG TTAAAAGCTA TAAATACTTT CAACAGATTA TCCACAGTTG 1380
TACATTATCC ACAATGTAAG TGTAACATGA TTAATTTTTT TCCTAAGGTT GGATATTTAG 1440
TTTCTCTAAA ATTTTTCACT ACTATGAAAA AAAGATTCAA CGTATATCTA AGTATATGCT 1500
AATCAATAAA TGCTTGTGAC CATGTGAGCT TTACATTAAA AACAAAAAGT TTTGAATATT 1560
TGGGTAAATG TTGAATTCCC ATCTTGATAG ATTCTTTCAA CCCTAAAAAT AAGATAGGAT 1620
TACTGACGTC TTTAAAATAA TGGAAATATT TATTGGCCCT AGTGTATCTG TGGTATCATT 1680
GACCTTTTAA AAAATCCAAA TCTAGATATG AGTCAGTGGT GTGAAAACAA AAAATAACAG 1740
AGAGTTTAAA ATTATTTATG 1760
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