| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01779 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:68849270-68851380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:68851205-68851226 | ACTTGCTTTCACTTTCCTCTA | + | 6.87 | | IRF2 | MA0051.1 | chr1:68851204-68851222 | AACTTGCTTTCACTTTCC | - | 7.36 | | STAT1 | MA0137.3 | chr1:68851065-68851076 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr1:68851062-68851076 | CCCTTTCCTGGAAA | - | 7.64 |
|
| | 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 |
| GH01I068383 | chr1 | 68848872 | 68851824 |
|
Enhancer Sequence | AAGATGTAGC AAAGCTTAAC ATGAAGGCTG GGCTACGGTC CTCAAAACCT AGTTCATAGA 60
GTAGTCCTGG GAATTAAATG ATGTAAGGCA TTAATTAAAT GATATAAGTG CTTAATTCAA 120
TGCCTGGCAT AAACGAACAA CTCAATAAAT GTTAGTTGCT ATTGTTGTTA ATTGCTATGA 180
CTTACTTGTT AGTGCCCTTA TGGTAACAAC TATTATTGCA AAATAATTAC AGAAAAGAAG 240
GGCTGATATT GGGAGAAAGA GGAGAGGATC TGGAAGTCCT GAAGAGGCTG AAGAAATAAT 300
AGACTGGGAG TAACTGAATG AGAATGTTGG AAGAAAGGTT GCAGTTAGTG AATGGAGTGT 360
TTGAATTTAA TATTTAGGAG ATAGAATAAT TCCAAGTAAT GATAGAAGTA TAGCAAACTG 420
GGATGGACGT GGAGTATGTG TGATGTGAAA TGGGAGATAG GAGAAGAAGG TCATTAACAC 480
TAAGGAAGCC AAAGGAGTCT GGAGAATCAG GTAGGGTATC CGTGTGGCTT TGGAACACTC 540
TCAGGATGAC AGCACAACTT AGACTACAGG AGGCAATGGA AAACACTAAT GTCTTTAATA 600
AAAGAAGGAA GTACCTGAAT CCTTGTTGGT AGGATTTCCA AGACTGAGAG TGTCTCTGGA 660
TCCTGTCGTT TTAGCAGAAC TACTCTGTGC ACTATTTATA CCCTTGTTGG AGTTCTCTCT 720
ACCTTCTAAC TTCAGGAAGT GATTTTATTG TGCCAGTTCC CAGAAAGCTG ATGGGGCAGT 780
GTATTCATGC CCAAGCTGGC TGTTTGGAAT ACATCTAATG TACCCATTCT TCCAGCCCAG 840
GCAAACTGCC CTTAAGAGCT ACTTGATCCA ACATCACGAA ATCTGTTCTC ATTCTAATTT 900
AGAATGCAGG AACTTGTGTG GTGACTCATA TGTTTGAAAA GCTCAAATTA AGTAGTGGTG 960
ATCTCAACCA TGATTCACTG ATGAGAACTG GAAAGTGATT CATCTCCTTT ATGTGCTTGT 1020
CCTTGGGAGT CTCCAGGCTT AAAGGTCTTC CAGAAACACA CTGCACTCAA GGAAAGACAC 1080
TGGGCCCTCC TGTGGTGGTA TTTTAGCAAT TACACAGAGG CATTCACTAC ATTTTTTTAC 1140
TAGGTCATTT CCTTTAGTTC ATTTTATTCC CATCTACAGT CCACAAGATG CTCTTGTGCT 1200
GTAATGATTC ACTGCCGATA AATGAAAAGT CAATGATACT TTTAGGTCAA AGGTGGGTGT 1260
ACATTTAGTA AACCATTGGT GCAGATTCAC AATTATCTAA TATGTAGGGA TAACTGTATT 1320
TTTCTTAGTA TGTACTTGTT ATCAAGGAGT AACTTTTTTC TTACCACAGT AACAGGGTTT 1380
GAATGTATTT TATATGATAC TGTCAGAGGC GTTTAAACCA GAGCAACTCC ATCTTGCATA 1440
GGCGCTGGGT AAAATAAGAC TGAGACCTAC TGGGCTGCAT TCCCAGGAAG TTAAGTCACT 1500
CTTAGTCACA GGATGAGATA GGAGGTTGGC ACAAGATATA GGACACAAAG ACCTTGCTGA 1560
TAAAACATTA TGTGGTCAAG AAGCCTGCCA AAACCCACCA AAACCAAGAT GGTGATGAAA 1620
GTGACCTCTG CTCTCCTCAC TGCTCATTAT ATGCCAATTA TAATGCATTA GCATGTTAAC 1680
AGTTACTCCC ACCAGTGCAG TGACAGCAGT TTACAAATGC CATGACAATG TCAAGAAGTT 1740
ACCCTGTATG GCTTCAAAAT GGGAGAATCC CTCAGTTCTG GGAATGGCCC ACCCCTTTCC 1800
TGGAAAACTC ATGAATAATC AACCTCTTGT TTAGCATATA ATCAAGAAAT AACTATAAGT 1860
ATCTCCTTAG TCCAGCAGCC CAAGCTGCTG CTCTGCCTAT AGGGTAGCCA TTCTTTATTG 1920
CTTTACTTTC TTAAAACTTG CTTTCACTTT CCTCTATGAG CTCACCCCAA ATTCTTTCTT 1980
GTGCAAGATC CAAGAACCCT GTCTTGGGGT CTGGATCAGG ACCCCTTTCT GGTAACAATA 2040
CCAAGAGGGA ATACTAATTA AAAAACTAGT TTAAAGTTAA GATAACTTAC ACTAAAATAA 2100
ACCAAAGATT 2110
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