| Tag | Content |
|---|
EnhancerAtlas ID | HS133-12519 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:36479210-36481490 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr17:36480478-36480489 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr17:36480478-36480488 | GCCCCGCCCC | + | 6.02 | | SP3 | MA0746.2 | chr17:36480477-36480490 | CGCCCCGCCCCCC | + | 6.11 | | ZNF263 | MA0528.1 | chr17:36480980-36481001 | CCCCCCTCTCCCACCTCCCTT | - | 6.23 | | ZNF263 | MA0528.1 | chr17:36480977-36480998 | CTTCCCCCCTCTCCCACCTCC | - | 6.95 | | ZNF740 | MA0753.2 | chr17:36480481-36480494 | CCGCCCCCCCCAC | + | 7.82 |
|
| | 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 |
| GH17I038323 | chr17 | 36479702 | 36481743 |
|
Enhancer Sequence | TGATTTCTAG CACCATTTGG AGATGGGGAC TGTTCTTTCC AGCCCAGTAT TGAAGGTGAG 60
TGTACAAAAG TATGAACCTG TGCAGAGGAA AATAGGCCAG CCCCTCCTTG TTCCTTAGCT 120
CCAGATGGGC TGTTAAAAGG GTGTGGGACC TCACATGCCC ATGTGTCCTA GGCCATCTGA 180
GTGTGACAAG AGAAATCACT TTGTTTTTGT TTTATTTTGT TTTTTAGAGA TGGAGTCTTG 240
CTCTGTCAGG CCCAGGCTGG AGTGCAGTGG CACGATCTCG GCTCACTGCA AGCTCCACCT 300
CCTGGATTCA AGCTATTCTC CTGCCTCAGC TTCCCATGTA GCTGGGACTA CAGGCATGTG 360
CCACCATGCC TGGCTGATTT TTGAATTTTT TTTTTAGTAG AGATGGGGTT TCACTATGTG 420
TTGGCCAGGC TGGTCTCGAA CTCCTGTCCT CAGGTGATCT GCCTGCCTCA TCCTCCCAAA 480
GTGCTGGGAT TACAGGTGTG AGTCACCATG CCTGGCCTGT TAAGTGTTAA CTATGGAAAC 540
AAAGGTATGT ATATTTAGGG AAGAGACAGC CCTGGTGTCT CTCATCAACC ACTCTCATCA 600
TGCTGCTTAG TCCCAACCTT TTTGGCTTAA AGTGTACATC ACTTTAATTA CTGCCCAAGT 660
GAGGTTTGGT CACATCCTAT TTGCCTGAGC CCTGGATTAA GGCAAAATGA GAAGGGACGT 720
GCTTTTGAGC AGGACCCACT GCCAGGGAGT ATGGAGGAAG GGGAAATAAT CCTTGCAGGG 780
TAAGGAAGCA AAGAAATGAA AAAAAAAAAA AAAGCACACT TAGTGGGTAA ATGATACATT 840
GATTCCTTTG AATATGTAAA AATAGTGCTT CAAATAAGCT GTTTCATCCC ACTCCCCTGG 900
ATATCTCAGG GTTCTCTAGA TAATCCTAAA TAGGAGCTAA GCAGTAGCTG CCACCAGAGA 960
GCCAGAGGAT GAGTGCAATT TCCATTTCCC CTTGGGATTA AATCCAGCTG AGCAAATGGC 1020
CTCCAGATGT GAGGGGCTGG CTAGAAGGAC CAGGCAGAGA CCATCTGCAG TGTCAGCACT 1080
GACCTGGGCA CTAGCAGAGC ATTAGCCAGA TAACCCAAAG TCCCAAGACT GCAGTGCACC 1140
TTGAGCTTTG GAGCAGGCAT TGTTCTTTCC TTATCTATCT TCTGTTACTG TTTAAAAATG 1200
TTAAAAAAAG ATAATCATGA ATAAGCTAGA GCCAACTGCA ATGTCAAGAA AAAGCATTCT 1260
TTATTTCCGC CCCGCCCCCC CCACCCCATG GTTTATTTCA CAAGAGTGTG TTTGGCGGCA 1320
ACTTTGCTGT TTCCAGCTAG ACCAGACCCA ATGGGATTGT TTTGGGGTGC ACAGCAAAAT 1380
CCACTTTAGC TCAGAAGCTG TAAGGCTAAC TAGCCAGAGC CCAGAACAAC AACACACTTC 1440
AATTACTGCT CCAAAAGCCC AGAATAAGGG CCCTAGGTAA GAGAATGAGG ACATCTGGTC 1500
CCCAAAGGAG AGTAGGTTAC TCCATTCCTC TGTTCCCTTT TGGAAATGGA GTACTTTTTT 1560
ACTTTCTCTG TGAAGTCCCA TAACCGCCCA GCATATTTAC ATGCAGACTA GATGTTAATG 1620
GCTCTTTTTC CCTTTGGGTA TTTGGTCTCC CTGTTTGTCT TTTTCTCCCC ATGAATGACA 1680
TCAATGTCTG TACTGTTGTA CTGTTAGAGG GCGTGACTTA CTGCCATCTT TAGTGCCCCT 1740
GTGCAGCTCT GCCTTCTCTA GCTGCCCCTT CCCCCCTCTC CCACCTCCCT TTGCCAATCT 1800
TGGGACTTCT TTGTATGTTT TTCTCCTTCT TCCTTTCCCT CTGGTATTAT CATCTAATCC 1860
CAGCAATTTG TAATCTAGTA CTGCTTAAGC AAGTGTAGCC TGAACTGACG AGAGAAGGGA 1920
GCCAAGAAAG AGAGAGCTCC CTAAGAAAGA AGGCTTTGTC TTCACACAGT GCCCTTTTCC 1980
CAGCTCTCAG GCTTCTAACT TGCCCTGTAG CACTCCTCTT TTAGAGGGCA GAAGAAGTAG 2040
AGTGCTGGCT GTGTACAGGA CTGCCTTTCT TGAGCTCCTC TGGAAGGAGA TTGATGTGGC 2100
CTCTTGTTAC TGAGCAAGTG ATTCTTGGGC GGGGAGGGGT GGGGGAGGGT GGATGGGTCT 2160
TGCATCAGAA CCAGAGATTC CCCTTGACTC CAGTTGCCTT GACAAAAGAG AGAGGTCCTG 2220
TTGATGGCAG CGCTGAAAAG CTAGGGGGAA GGAAATGAGC CAGTGAGACG AGCTCTGGAG 2280
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