| Tag | Content |
|---|
EnhancerAtlas ID | HS133-06768 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:290620-292100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr12:291882-291893 | CTAATCCCCTT | - | 6.32 | | ZNF263 | MA0528.1 | chr12:291625-291646 | TCCTCCCCTGCGCCCTCCCTC | - | 6.11 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 291440 | 291523 | | chr12 | 291572 | 292069 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I000182 | chr12 | 291400 | 292062 |
|
Enhancer Sequence | GTCTTTGTAG AGACGGAGTC TCACTACGTT GCCCAGGCTG GTCTCAAACT CCTGGCCTCA 60
AGGGATCCAC CCACCTCGGC CTAGGCTTGC CATTTTTAAA TAATGGAATG GACTCCATGG 120
CCTATTGCAC AGCAGTCCCA AGGAGTCCAG GGGCTAACAG CCTTTCACGT CTCAGCGTGA 180
ACCCCACAGA ACGGAAGTGA GATTGATTTC TCCTTCAGGG GGCTGGCACT ACATGGCTGC 240
GGCCCTCGGC ATGCCCCCTC CCATCCCAGC TCTGACAGAT GTGGCCAATT GATCACTGCT 300
TTCTGGGAGT CACCATCAAT CACATGTGCT GACTCCAGGA TGAAAGAACT TGCCAACCGC 360
CCCGTGGTGT CCTCATGGAG ACACCTGGAA GGAAGGCATT TTGACGGGAG GTAGCTTAGA 420
GCAGGGGGCA GCAGGCGGGA GGTGTGGCCC TCCTAGTGCC ACTGCTCTCA GGTCACTTGC 480
GGACAGCAGC TCTGGGGGTG CTGGCTTTGG CTCCTTAGCT CTGCCGCTCA GGGACTCAGG 540
GCTGCTTCCT GCCAGGACTC CTCACTACTC AGCAACCGGT CGACTACCCT GTGCACCAGG 600
TCCCCTCACT CACCTTCCTC GGGGTGAGCC ACATGGCCCC CGGTGTCACA GATGAAGGTC 660
TGAAGACGCC CAGGCAAGAA GGACGCTCCG TCCAGGGCGG AGCCTTGGGA GCAAAGGCAG 720
ACCCCGTGGA GGGCAAGGGA GGTGGTCCTT CCAGGAGAAC GTGAGGCCCA GCCAGCGCCC 780
AGCGGCCTGG AGCCGCAGGC TGAGTTCTGA TCTGCTCCCC TTCCCGTCCC AGGACGGCAG 840
CCAGGCCCCA AGATAGACCA AGCCCAGGTC AGAGTCAGGG AGGTTAAATG AGGGCGCAGG 900
AATGGGGGGT GCAGAGGGAC AGGTCCAGAA GTGGTTCTGC CAGAATTCCC TTCTGGATGG 960
GCTGGAGGAG AGGGAGCTGG AGCTCAGCGG GTGGGCGGAG TGCTCTCCTC CCCTGCGCCC 1020
TCCCTCCCGT GCCCCTGCAG GGCTGCACGG GTTCCCTCCC TAGGGAACCA GGCTGCCTAA 1080
CCCACCAGCC GGCCCCTAGC ACCTCAGCGC TTCCTGCTCC CATGACCCTA AGGACTAAGT 1140
GACCTCAAGC CTGGCTCTGG GAAAACTGTG GGAACCGGCT GCTGGGAAGA CGACCTGGCT 1200
GTTACTCCCA CGTTTCCAAC TGCCTAGACA GACCTGCCCT GCCCTCCTTT CCTCAAGAAA 1260
CCCTAATCCC CTTTCCTTCT GAGACATCTA GGGTAGGAGT CAGCCTCCCT CCCTGCACCC 1320
TCAGAGGGAA TGGAAGGCAG GGGAGTCATA CAGCAGTGCC AGGCCTGCAG GCTGAGTCAC 1380
AGGCCAGTCA TCCTTCTATG GCTAAGGGGA CTACTTCACT TAAGAGGTTA AAAAAGAAGA 1440
ACAGAATAAG CCCAAAGGAA AGAAACAATA AAGACAAAAG 1480
|
