| Tag | Content |
|---|
EnhancerAtlas ID | HS133-22918 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:127915690-127918210 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr3:127915863-127915875 | TGCTGTGATTTC | - | 6.22 | | Gfi1b | MA0483.1 | chr3:127915863-127915874 | TGCTGTGATTT | - | 6.62 | | IRF1 | MA0050.2 | chr3:127915841-127915862 | GAATACTTTCTTTTTCTCTTA | + | 6.03 | | Stat6 | MA0520.1 | chr3:127917190-127917205 | TTCTTCCTGAGAAGT | + | 6.55 | | ZNF263 | MA0528.1 | chr3:127916989-127917010 | GGGGGATGAAAGGGAAGGAGA | + | 6.7 |
|
| | 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 |
| GH03I128197 | chr3 | 127916406 | 127917600 |
|
Enhancer Sequence | CACAGTGTGG GGCATGCACT CAGCAAATAG TTGCCATTAT TATTATTGGT GACAGCAGTG 60
GCAGCTTTGT CTTGTGGCTC CTCTAGGGAG AGTTTGGATG CTCGCAGTAT GTTAAGAATT 120
TGCAGCCCAG CTCTGGCCTC GTTTTTTAAA TGAATACTTT CTTTTTCTCT TATTGCTGTG 180
ATTTCTTCTT TTGCATTTTT CCTCTTTGTT CTGTGTACTT TTGTAAGTTG CTTTACATCG 240
TTTTTGCAGT AAGGCAGATT ATAAATAAAT AAACACTGAC TATTCCCTCT AGTGTTGGTT 300
GTTTAGGTTG TTTCTGATTT CTTGCTATTG TGAATCATTC TGCATAGAAT ATCTTAGTGC 360
ATCAGGGTCT GTCCTAGGTT GGATTATTTG CTGGGGCTAG AATCCTGGAG GCGGAAATAC 420
GCATTTTGTT TTTCTTTTTT TTGAGACGGA GTCTCGCTCT GTTGCCACGC TGTAGTGCAG 480
TGGTGCGATC TCGGCTCACT GCAACCTCTG CTTTCCGGGT TCCAGCAATT CTTCTGCCTC 540
AGCCTCCCAA GTAGCTGGGA TTACAGGCAC ATGCCATCAC GCCCAGCTAA TTTTTTTGTA 600
TTTTTAGTAG AGACAGGGTT TCACCATATT GGCCAGGCTG ATTTCGAACT CCTGACCTCA 660
AGTGACCTGG CCATCTTGGC CACCTAAAGT GCTAGGATTA CAGGTGTGAG CCACTGCGCC 720
CGGCCGGAAA TACGCATTTT TACATCTCTG ATCCAATTTC TTCTCAGAAG GCTGTACCAA 780
TCTACACTCC CACCATTAAC GGTACGAGAA GACCAGTGCC ACTGACTCCA TGACTGACTG 840
GCCTCTTTCT TTCAAGCCCC GTTTCTTGTC ATGGCCCAGG GTAGCAACAA TCTGATTCTC 900
ACCTGGATGC TGTGTTCTGC ATCATCATCA GTAAATGGAG CTCAGGGTTG AGGTCTGCCC 960
CAGGTCCCCC GGTTTTGGTA AATCTTATTT CTGATGGGAA GGCAGTCCTG TCGCCAGCCA 1020
GTCCTGCCTG CATAGATTGC CCTCTCTGCT AAACAATGGA CACATTCAGA CCCGACTCGT 1080
GTTTTCAGTT ATTAAAAAAC TGAGCCGTCT GTCTCTGCCT GTGACTTTAA TCTTTAAGCC 1140
TTTATTCCCT TTACCCCATC CCCCTTCCCT TAACCTTTTG TTTGTGCAGT TCCGAGCTCA 1200
GGGATACGTG GGTCCAAGAC TTTCTGAATG TACTGTGGCT TCCCCTGACA GCTACAGATG 1260
GTTGTAGCCC TGAGTGATGT TGTTTCAGGG TAGGCAAGGG GGGGATGAAA GGGAAGGAGA 1320
AGAGAGGTCA GCTCTTCTTG CCTCCAGCAA TCATTTGAAC TTTGCCAAAA CTATTTTTAC 1380
ATAGCTCTGG AGTGGAGTGC CTCCGTTCCA TTCTCTCCCC ATTTTCAAAT TTGGTAGACT 1440
TGTACCGTTT CTGAGTTGCT TAGGCTTAAT AAGTTTACAT CTTACAGTGC CTCTTAGCAT 1500
TTCTTCCTGA GAAGTAGTTC TTGTGGTTGA ATTATGTATA TGTGTGTCTA AAAGCAAAAG 1560
TCCCAAGAAA GGATCTTCAC CCCAACCCCC TTAAAACACA ACCAGAAAGC TCAGAACACA 1620
ACAACATCTT CCATTTCAGA AAGGGCACTC TTCCGGCAGC ACATGTGGTT CTCAGTGTCT 1680
TCTTGCACAA GGCCAGCCAG AGAATGCTGG ATGTAAAAAC CAGTGACAGG GCCATGAGCT 1740
TGGCTGACAG GGAGCATTAG GAAACCATCC TCTCTTTTGC AGAGACACTG GGGACATTCC 1800
TTTCTGAAGA AGGCTCCTTG CATACAAAAA GAATGGTCTT TAAGAGTGTT GCTGGCACCT 1860
TTCTGTGAAG AGCCACACAA TGCAGAGGGA GGGAACCTAT CACTTGGATG TGGAGGTGCA 1920
GGTCTGAAGG CCAGGAAGGA GACATTTTTT CATATGTGTG TTTTTTTTTT CTTAAAGACT 1980
TTCTGTTTTT TTTTCTTTTT TTGAGGTGGA GTCTCACCCT GTCGCCCATG CTGGAGTGCG 2040
GTGGCACTAT CTTGGCTCAC TGCAACCTCC ACCTCCCAGG TTCAAGCGAT TTTCTTGCCT 2100
CAGCCTTCTG AGTACCTGGG ACTATAGGCA TGCGCCACCG CACCCAGCTA ATTTTTGTAT 2160
TTTTAGTAGA GACAGGGTTT CACTGTGTTG ACCAGGCTGG TCTCCATCTC CTGACCTCAG 2220
GTGATCCGCC TGCCTCGGTC TCCCAAAGTG CTGGGATTAC AGGCTTGAGC TACCACACCT 2280
GGCCTGTGTG TATGTTTTTT CAAGTGTGTG CATTTTTTGT GCATTTTTAC ATGTCAACAC 2340
ACCCTGTTTG TTTTTAAACC TTTTTTCTCA CTACAAAGCT TCTATGACTC CAGCATTTTA 2400
TAAATGCCTT CAGAGAATGC AAGAGCCTCC TCACCCCTTT ACGGTGATGT TAACAGAGGG 2460
TTGGTGCCTA TTCATCTGAC TTTGTCCACA TATATGTATA TTTATGCTTA TGTTAGTCTA 2520
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