| Tag | Content |
|---|
EnhancerAtlas ID | HS133-22440 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:64093980-64096400 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr3:64095586-64095597 | TGTGGATTGGA | - | 6.62 | | ZNF263 | MA0528.1 | chr3:64095263-64095284 | AGGGGTGGGGGAGGAGGGGAG | + | 6.17 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I064109 | chr3 | 64094738 | 64096095 |
|
Enhancer Sequence | GGTACATATT TGTTTGTTTG AAGCATGTGT GGCGGTAGCT TGATCAGGTC CCTTGGGATC 60
CTTTCTCCAA CTAAGTCAAT CGATTTCCTC AACATCCCGA ACTTCAAATT GGCAACAGCT 120
GGAGAGATAC TGTCATCTGG GCAGTGGAGC TTAAACGCCA CCACATGTTT CTTGGTGACA 180
GGGCATGGAA TGGCTCAAAC AGAGTATGAC AAAGAAGGCT GGGGGTGGGG ACAGAAAGAG 240
GAGAGTGGGA CAATATGAAT GCACTCGAAA GTGTGATCTG TGGACCAGCC ACGATGCCAT 300
CCCTTGGGAG CTGGTTGCAG ACTCTCAGGC CCTCACCGGA CTTGCAGAAT TCAAATCCAC 360
ATTTGAACGA GATCCCTGGT GATTCTCATG TTCATGAGAG TTAGAGGAAC ACCAAGATGA 420
TGGGAGTTTC AAGGACGATT TTCTTTGCAA CACAAGGGTG CTTCTACTCC AGGAAACAAG 480
ACCCTCACAC TCTCAGAGAC TCTAATTCAG GGTTTCCCAA CCTCAGTACT ACTGACATTT 540
CGGGCTGGAT AATTCTTTGT TTGGTGGGCT GTCCTGTGCA CTTCAGGATG TTCAGCAGTA 600
TCTCTGGACT CTACCCACTA GATGCCAGTC ACACATCCCT CTGGTTGTGA CAGCCCCGAA 660
ATGTCTCCAA ACAGTGCCAA ATGTCCCTGG AGGGCAAAAT CGCCCCCAAC TGAGGACCGC 720
TGCTCTAACA GATCCTGTCC TCCACCTGCT GCTTGACCAT AGCCCAAGGG GAGCTCTGTT 780
CCTGTCCACC CAGTTGTTGG AGTGAGTTAA ACCTGCTCTA CCCCATCCTG CAGACAGGAG 840
CCTCGTCACG ATGGGGGTTG CCGCTCCTTC TTTCTAGAGA AGGATTATCA GGGCTCTGCC 900
TGGTTGGGTG TGGTATGTCC CCAAAACTGG GGAACTCTAA AAGTTATTTT CTCTCTAAAC 960
TCTTCTCAGA AAATTCACAT TCCTTTCTCT CAGTGGCTAT CAAGAACTCC CCAGTTAAGG 1020
CCTTTGCTGT CTAATTTTCC TGGCAGGTTT GAAGCTTTTG AAATCCTGAG TTTTTGATGT 1080
ATCTCTTTTA CTTCCTTACT CCAGCCACTG GCCTATCTAG CAGGTCTCAG GTGATCAGCA 1140
GATCACAAGT TGGCTTGCAG TCAGTTACAC ATCTGTCATC TGCTCTGGTG CTACCAGGAT 1200
CAGTGCTGGT AGTCTAAGGA ATGATTTCCT CTGCCAGCTG CACTGGGGAA GGGAAAGGGA 1260
AAGGGGAGGC CAAGCCCTGG GGCAGGGGTG GGGGAGGAGG GGAGTGTGCA TAACTTCTTA 1320
CTTCACACTC CCACCCCCAG GCTTGGCCTG CCTTCCCTCT CAGTCAGGCA TGGGCTGTTT 1380
AGGCCCAAAC TAAATAACAG CCTCTTTACA ACCAGCTGCT TCCAAAGAGG GTCATGGACT 1440
GATCTTGGTT TTCCCAACAA TAGCGGCTTT GTTTTTTAGC AGCATTCATT CTAGGGACTT 1500
GCCTTTGAAC TGGAGGTTGG GGAGTGACAA GCATTATAAT GGGACTAGAA TCACTTCTCT 1560
GACAGACCCA GTACAGTTAC AAGGACAAGT CAGATAAAAA CTTGAGTGTG GATTGGAGGT 1620
TTCTTACCTT CTATCCCTTT CCTTGCTCAT CCTATTAACT TCCGGATAAA TCAGTGACCC 1680
CAATAAAGAT GGAGTCAATT TTAACTAAAA CCACTTGTAA AAGTGAAGGA GGAAACCAGG 1740
AAGGGACATC TTCCAGAATC ATGTGGAGTC AGTTTTAACT AGTACCACTC AGCTCCATGG 1800
GGGATTCTGG TTGTATTGCC ACAAAGCATA TTGCTAATTG AAAGGATACA CAACAAATTC 1860
AGACCAGTTG AAGATTTTTT TGCCAGAGTT TGCTCTGGGT TTACACTGAC CCCATGCTGC 1920
TTTCTAGAAC CCATTAGTCT GGGTCAACAA GCAGACCATG CTGTATTTAC TTGGGAAACA 1980
CTTGACTACA GGAGGACAAA AGCTAAATGG CTCCCAAGTG GTAGAGAGTG GGCAGCCAAG 2040
AACCTGGGGA CCCACTGAGT TGCTTCAAAG ATCTTTGACA AAGCCCTGCT ATTGCCAGGC 2100
ACTGGGAGCA CAACTGTGAA CAAGGCCCTT TAAGAGGACA ACGTAGAAGG ATATGACCTA 2160
GTGCAGGGAG AACAGATAAC CAAGTCAGCA TAGCAAGGTG ACCGTTACAG ATAATAATCA 2220
CTAGGAAGGA AATAAAGGGG ATGCTATGGC AGAGAATAAA GACTGGACCT ACTTTGAGTG 2280
CTGGAAAAGA ACTCTGTGTT GGTGATGACT ATGGGGAGAC CTAAAGGATG AGAAGGAGCC 2340
CACCCAGCCA AGGGCAGGGA AAAGTGTTCC AGGCAGAGGG AGCAAGAATA TTTTGTACTA 2400
GAGAAGGTGC CACGAGCTCT 2420
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