| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00372 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:15068090-15069970 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid3b | MA0601.1 | chr1:15069954-15069965 | ATATTAATTAT | + | 6.02 | | HEY2 | MA0649.1 | chr1:15069791-15069801 | GACACGTGCC | + | 6.02 | | NFIA | MA0670.1 | chr1:15069420-15069430 | ACTTGGCACC | - | 6.02 | | Npas2 | MA0626.1 | chr1:15069791-15069801 | GACACGTGCC | - | 6.02 | | SREBF2 | MA0596.1 | chr1:15069177-15069187 | ATCACCCCAT | - | 6.02 | | ZNF263 | MA0528.1 | chr1:15068138-15068159 | AAAGGAGAGGGAGGGAGAAGG | + | 6.52 |
|
| | 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 |
| GH01I014740 | chr1 | 15067455 | 15070250 |
|
Enhancer Sequence | ATCTTTTTAT TTTTCTCTTA CATGAGGCTG AGCTACTTGC TGAACTGAAA AGGAGAGGGA 60
GGGAGAAGGG GCACTTCCCC CCGGGGTTTC AAGACCTGCT GAGCTTCATA GCCAAGAGGT 120
TCTCACTCCC CACTCAAGTG TCAGCTTTCC AGAATGGCCC CTTGAAGACA AAAACTCTTT 180
CAAGGCATAT TAAACAATAG CAAACTCTGA TAAAATTCCA TTCTGGTGGC ATGTTTTATG 240
AGAAACTGAT GAGGGGCCCT GAAATGCATC TCAACCTTGA TGTTTGAGCC AGAATCCAAA 300
TATTCCCTTT CTGTTAACCA ATTCAATGTT GCTTCTCTCT TGTGGTTGTT TTTTTTTGGG 360
TTGTTTTTTG TTTTGTTTAG GATTTTCCTT GTGGGAAGCC ACATTCACCT TCTTGATACT 420
ATGAAATGGC TATACAGAAA AATAGAACCA TCCCCAAGCA AAGATTCCTC CCCCTTTGGA 480
ATTGTCCCAG TGTGGACAGC ACTTCCCTCC AACTTTGGAT GAACAGAACA AACGAAAGGA 540
GGAACTGTGA GTGGGGTCCT CTCCAACTGC TATAATGTCA GCTCCAGGAA AGCAGTGACC 600
TTGTCCGTCC TGTTCACTGC CTGTTCCCAG CATCTAGAAG AGGGCCTGGC TCATAGTAGG 660
CACTGAATAA ATATTTGTGA AGAAGCTGCT AGATTGCAGG CTTTGTGATG GCAAGGACTC 720
TGCCTAGGTC TGTGTTATTC ATGAATGTGT CCCTCCCACT TAAGAGCACA GCAGGCACAA 780
AATAGAAGCT TATTCATTCA TTGAGCAACT ACCATATGCC AGAGATGACT CAGGCACTGA 840
ATAAATACTT GTTGGATTAA CTAAGTGCAT TCTTGCGTAC GTGCTTGAAT GAATGAAGGA 900
ATGAGCGAAT GAAAAAAAAA CCAATGAGTC AGTTCATCCG CCAGCAATAA CCAATCTCGC 960
CTCTCTGTGC TGCAGTCTTG GGACAATAAG CCTGGAGGTT TCTCTCCCTG TGCTTTTTCT 1020
CGCTTGTTGT GATATCCCTG CCTACCAAAA CTCCCAAGAA GTGTCAGCTC CAATGATGTT 1080
TCTTTGAATC ACCCCATCTG GCAAGATGCA AACACTCTTG CTTTTGAATT GCTTTGTCAC 1140
TTTCTGTCTT AGCTGTTGAG CACAGTTCAA AACCCATTTG CTGAGCCTGT CCTGTGGACA 1200
GCCATGGTGG CAGGAGCCAG GGATGTAGAA GTGACCCTGG AGTCACCAGG GTTCAGTGTG 1260
TGTCTTGCCT GCCTGGATTG TACAAGCACC CACGGCTCAG AGACGGAGAC TTCCTCCTCT 1320
CTGTAACTGC ACTTGGCACC TGGTAGTGAG TCTGGTCAAA CAGATGCTCC TGCACTCACC 1380
AGTGAATAGA CCCATAAGAT GTGCCGCCTT TGAGATCTTT GCTTTGGTGG ATTTGAAATA 1440
TGGGAGGAAG AGCTGAGCTG CACTGTGTGT GGGCCAGAGT GGTGCGTCGC AGGCATGAAG 1500
AGGCCAGGAG TAGGGAGAGT TCCATGGGGG TCAGGATCAG AGAGGTCCAT AGTAGGTTCA 1560
GGTGTGGTGG CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGTGG GAGGATCACT 1620
TGAGGTCAGG AGTTCGAGAC CAGCCTGGCC AACATGGTGA AACTGTCTCA ACTAAAAATA 1680
CAAATATTAG CCGGGCGTGG TGACACGTGC CTGTAATCCC AGCTACTCTG GAGGCTGAGG 1740
CAGGAGAATC ACTTGAACCT GGGAGGCGGA GGTTACAGTG AGCTGAGATC GCGCCACTGC 1800
ACTCTAGCCT GGGGGACTGA GCGAGACTCT GTCTCAAAAA AAAAAAAAAG TACATACAAT 1860
GCAGATATTA ATTATTCATT 1880
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