| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26494 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:20680260-20682880 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr6:20681283-20681304 | ACCCAGTTTCAGTTTCATCTG | + | 6.35 | | IRF1 | MA0050.2 | chr6:20680267-20680288 | CATCACTTTCTCTTTGACTTT | + | 6.41 | | IRF8 | MA0652.1 | chr6:20681287-20681301 | AGTTTCAGTTTCAT | - | 6.74 | | IRF9 | MA0653.1 | chr6:20681287-20681302 | AGTTTCAGTTTCATC | - | 6.04 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I020680 | chr6 | 20680857 | 20681431 |
|
Enhancer Sequence | CTGATTCCAT CACTTTCTCT TTGACTTTTA ATTTTTTTTA ATTTTTATTT TTTTCTGAGA 60
CAAGCTCTTG CTCTGTTGCC CAGGTTGAAG TGTAGTGGCG TAATCTTGGT TTACTACAGC 120
CTCCACCTCC CAGGTCAAGT GTTTCTTGTG CCTCAGCCTC CTGAATAGCT AGGATTACAG 180
GTGCCCACCA CCATGCCTGG CTAATTTTTG TGTTTTTAGT AGAGACGGGG TTTTGCCATG 240
TTGGCCAGGC TGGTCTCGAA CTCCTGGCCT CAAGTGATCT GCATGCTTCA GCCTCCCAAA 300
GTCCTGGGAT TCCAGGCGTG AGCCACCACA CCCGGTCTAA TTTTGTTGAG TTTTAAAATA 360
ATTTTTATTT AGAATTTTAT GTAGGTGTTT TTAAACATAT GACATTATAT TTGAAATTTC 420
TTACAAATAT TTAGTAAAGG AAGGAAAACT AAAGAAGAAT TTCCTGACAA TAAAGCGCTG 480
TTAGCAATGT TTGATTCCTT ACATTCGGTG CTCAAACCAT TACTATTCTA GGACTGGTCC 540
TTTTTAAGGA TGGTTGAAAC TAGGACAGAT TGTCACTTGT CTGGAATTGT TCTTTCTATA 600
AGCAAGACTT TATTAATACT GAATGTTATC TCCCTCTGTC TCTGTCTGTG ATTCTCTTGA 660
AAGTGCTTCA TTCTGACTGA AGGAAAACTT TTGCTTTCTG CATGGAGCTT TGTATAGAAA 720
CCCGGCACGA CAGGGCACTT TCGGGTCATG CCTTGAGTCT TAAGAAATAT TGAAAAATAT 780
AATCTAACAA TGATGCTTCT GTTCAGCAAG GCAAGGAATT TATAACAGGG CAAAACTGAA 840
ACCTGTTTCT TGTTTGCTAG CCCATAAGGA GGCAGCTTGT TTTTATCATC AGTTTCCTGA 900
CATCAGGATG TGACTTCGAG AAGAGGAAAA TAACACTTAT TGGCATCAAA GATACTAAAG 960
TATTTAATGC CTTAAATGAA TAATCAGTAT ATGTGAACAA TGAAAACACA GATGAGGAAG 1020
GATACCCAGT TTCAGTTTCA TCTGTTGTAT CATGTTAGTT GGAGATATTT AGCTTAAGCC 1080
TCTTCCCTGT TGGTCCACTT TACCCTAGTT GTTTCACTGT TGTGAATGCA TTTACAATTA 1140
TTTTAAAAGA TGGCCTCATT CTGTAGGTGA ATCCCTGTAA AGAACATTGT AGAAGGTTAT 1200
TATAACAACT CCTAAGCATA AGCTGGAGTC TAAAATGTTT CTAGGCAGCA ACAGTCATAT 1260
GTATGCTTGA CCTTTGGGAG ATCTGGTTCT TTCCTGTTGC TTGTTTTTAC CCTGGCACTG 1320
TCACCCACTT GTGCCCAGGC TAGTTTCAAC CACTGTTTGC CTGAGCCTAC ATTTTGTGTT 1380
TTTTTCCATT TTAGCATGTT TTACAAATTT ATTGAATTAC ACTTTGTACC AGGTATTGTG 1440
TTAGGGGGCA GGTATAAAAG CAGAGTTCTC ATCTGTTATT TGATAGGAAA GACAGTGTGA 1500
CTGTTATCAG TTTACTTATT CTCAGCCTGC AGCCCAGCCT TGTTTGCCTT GCCTTGGGTG 1560
ACATAACTGG ACTCTGTAAT AGCTGTTCTT TGTCAGCTGC TATAATGTTA GTAGATGGTC 1620
TTGGTGGGGA ATTGCAAAGT GGTGGCAGCA GGAAAGCACT TGTCTTCTGG GTTCCAGTTT 1680
TCCTCCATTT TTAATTCACT CCAGAAGCGA GAGATGGGTG CATGGAAGGC CTGGTGGAGC 1740
TCATAGGATA GTATCGATAC TGCCTCCTTT CCCATGACAT TACAGACTGT CTTAGTTTGC 1800
TCAGGCTGCT CTTACAAAAT ACCATAGAGC AGGTGGGTTA TAAACGACAG AAATTTAATT 1860
CTCACAATAC TGGAGGCTGG GAATTCCAAG AATAAGACGC CAGCAGATTT GATGTCTAGT 1920
GAGAACTCAC TTCATGGTTC ATAGATGGCA AGTTATAGCT GTGTCCTCAC ACAGTGGAAG 1980
GGGCAAGGCA GCTAGCTTTA TGGGGTCTCA TTTATAAGGG CACTATCTCA TTAATGAGGG 2040
TCCCACCCTC ATGACCTAAT CACCTCTCAG GAGCTCCATG TCCTAATATC ACATTGGTGA 2100
TTATATTGTA GCATATGAAT TTGGGGGGGA CACAAGCATT CAGACAGTAA CACAGGCCAT 2160
CTCCCTCAAG AAACCCTGGT TCTAGCTGTA ATAGTCTGTA CTTATCTGAT CTGCCGTTCC 2220
TTCTCTGCCT AGATGACATT TATTAAAATA TCTTTTATTA TCTAACAGCA CTTCCCTCTT 2280
GCAGTCTTCC TTAAACATCA GCCTGTATTA GTCTGTTCTC ACACTGCTAT AAAGACATAC 2340
CTGAGACTGG ATAATTTATG GTGAAACGAG GTTTAATTGA CCCAGGGTTC CACAGCTGGT 2400
ATAGGAAGCA TGGCTGGAGA GGCCTTAGGA AACTTACAAT CATGGCAGAA GGTGAAGAGG 2460
AAGCAGGCAC AATCTTCACA TGGCAGGGCA GGAGGAGATG GGAGTGCTAC ACACTTTTAA 2520
ACAATGAGAT CTCGTGATAA CTCTATCAGG AGAACAGCAA GGGGGATGTC TGCCCCCATG 2580
ATTCGATCAC CTCCCATCAG GCCCCTCCTC CAACAACGGG 2620
|
