| Tag | Content |
|---|
EnhancerAtlas ID | HS133-07052 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:12111190-12112820 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr12:12112138-12112150 | TGTTTACTTTGT | + | 6.18 | | NKX2-3 | MA0672.1 | chr12:12112739-12112749 | TTCAAGTGGT | - | 6.02 |
|
| | 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 |
| GH12I011958 | chr12 | 12110940 | 12112751 |
|
Enhancer Sequence | CGCTCCTTGA ATTCGCCTCT GATATTGCAC TTGTGTCTGC ATATTGACAG GTTTATGGAA 60
GACACTTCCT AGCCATCTTG TGAGCTCCTT GAAGGAACTG TGTCTTTATC TGTATAGCCC 120
CACCTAGCAG ATGCTCAAGG CATGCTTGTG GAATGAATAA GGGAACAGAT CATTTCTTCT 180
GAGCTGTTTG CAGTCTGGCT AAGCCAATTG AAAGAATGCC TTCTCTTGCA ATCTACAAAT 240
TGAAAAGCCT GTGAGACCCT CAGGACACTC AGGCAAGTTT TCCAGCATAT GTGACAATAC 300
CAAGCCTTAG TGCATTTGCC TCTCACGTGG AGGAGTCTCT TCTAAAAATG AAACAGAGAT 360
GAAGGGTGAG ACTCTTACAG TGGTTCAACT CCCCTAAGAT CCTCTTGTGA TTTAGAAGCA 420
TCTTGGAAAG AAATCCTTGA CACTCGCCTC GCCCACCCTG AGCTATAAGG TAAAGCTCTC 480
GGTGGTAAAC GTGGCTCCCT GGTAGGGAGA CTTCTTTTAT CCTCATTGTT TCTGGAGGGG 540
GAAGTGTTAG CACAGAGACT CCCTGGGAAA CCCGAGGATG CCTCACCACC TCACCATAAC 600
AGCAGGAAAC CCAGAAATGA TTCACAGCTG AAACCTCTGG CCCACATCGA CACATCACAT 660
CACATGGTTG TTTCAACTGG AAACCAAACA GCCATCTGGG CATGATTATC TGTATTTTTG 720
TGAAGGTGTA AATACACAGT GAGTAGGAAG AGTCCAATAA AACCTATTAT AATGTTGGTG 780
GTGGGCACCA CAAAGAGAGC ACCCCTTAAT AGACATTCCC TGGTCCAGTG AAAGACATAC 840
TTTGTACTGA GTCCCGCGCC TGGGAGACCT TCCAGGAAAG TAAATCCCCA GGAGAGAGAG 900
GCATTTCCCA GTAGGTGCTT TGCTTTTTGG TTGTTTTCTT TTCTTGGTTG TTTACTTTGT 960
TCTACTTTGT TTTTACTACA GTTCTGTCCT ACTGGTGGCG GAGTGGGACT CCTTCATGAT 1020
GTGGCACAGT TTCCTTGAGT TTTAGGAAGA AACGGCCCAT GTGGCAGATT CAGAAACAAT 1080
GAATCAGCAC CTAAACAAAC AGGAAGGTAA GCGGCCCTCC CAAGGTCACC TGGGTAGTGG 1140
CAGGGTGTGA ACCAGAGTCC AGGTGTCCTG ACCACCCACC ACCGCCTGTC CTCCTCCCTC 1200
ATACAAGATC CCTTCTAGGC CAGCGCTGAG AATAAAGGCA GCGGCATCAT GGGGAGGGGG 1260
TGAGGACAGA AGGGTCAGGG AAGGCACTGG GAGGGAGAGG CAATCCCAAC CCAACTCCAA 1320
CAGCCTAGGG TCAAAGCCCA GCTCCACTCC TGGCAGCTGT GAGACTTTGG TGCATTTAAT 1380
GTCCTTGAGC CTCTATTTCT TCACCTGGAA AATGGGATTG ATGACAATAT GCGTCCCTCC 1440
AACAACTAAA TGGCACATCA AAGCTTTGGT TAAAGGGGTT GGCACATCGT GAGGACCACG 1500
TCAGCTCTTA ATACTCCAAT GATGGCTTCC CTATAAGTGC AGAGTCTTCT TCAAGTGGTG 1560
GTTAGCACGG GTTTTGCCTG TTCCTTTAAT CATGGCTGTG AATTTGCTCC GGCACCATTG 1620
TTCCCAAAGT 1630
|
