| Tag | Content |
|---|
EnhancerAtlas ID | HS002-00021 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:5976430-5978240 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:5978165-5978183 | GCAGGGAAGGAAGGAATC | + | 6.21 | | MYCN | MA0104.4 | chr1:5977874-5977886 | GGCCACGTGGCT | + | 6.37 | | MYCN | MA0104.4 | chr1:5977874-5977886 | GGCCACGTGGCT | - | 6.37 | | Nr2f6(var.2) | MA0728.1 | chr1:5976851-5976866 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr1:5977464-5977485 | AGGGGAGGGGAGGGGGTAGGG | + | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I005918 | chr1 | 5976623 | 5976770 | | GH01I005917 | chr1 | 5977721 | 5977870 |
|
Enhancer Sequence | ATAAGTTAAA CACTAGTGGG TATTTAAAAG TCTCTTACAT TGGGTTTTGA GAGGCAATGT 60
CTTCCAATGC TTGGAACCTG GGCTGAAGGT AATCATTTAA TGTGACATGA ATGCAGCCAT 120
AAATCCAAAT TAAATAAACT CAGTGAAATC AGGGTCCATC CATGTAGATT TGCTGGTCCC 180
CAAACAGTGA CTGAGAAGTA GATTATGCTG CTACAGCTCA TTTGCACCAC CGTTCAACTC 240
CTGGTCCTTC CAGTAACCAA GGCACACTCC TCTCTGCCAA GGATATGACA GTAAATCTTC 300
TGGTGAGGAA CTCAAAGCAT GGTTCCCCAC AGCTCTGCAT CTTAAGAAGT CAAGCTAGGC 360
CGGGTGCAGT GGCTCATGCC TGTAATCCCA GCATTCTGGG GCCAAGGTGG GCGGATCACC 420
TGAGGTCAGG AGTTCAAGAG CAGCCTGGCC AACATGGCGA AACCCCATCT CTACTAAAAG 480
CACAGCAGGC TTCTAGAAGG AGGACAGGCT GCTTCTTACC TGTCTTCGTC CTTCTCAAAC 540
AAAAGAAAGA GTCACAGGAA CTACTCAAGT CTATGCATTC ACTGACGGCA AAATGCAAGA 600
ATAGCTGGGC AAAGCTGGAA TGCAAGAGTG CAGCCAAAGC GGCAGTGGCA GGGAAAGACC 660
CTGGACTGGG ATCGGGAGAC CAGGAGCCCC AACCCAGAGG CAGCCACTAT CTGTCAACTT 720
CACCGACCCT GAATCCGTAC TCTCTTCTGG TGGTTTTCCT TTAGGGAATC ACCCTCCCAG 780
CCCTTAACCA TACAGTCAGG GGTGGCCCCA ACCCCCACAC CAAGAAGGGT GTGTGACCAA 840
GGCCAACTGT CCCCACCCCC ATCCCCATCA GGTGTTACAC AGTAAAGACA GGAGGACTCC 900
CACTGGAACA ACTGAGTCAA TCAGGGCCTT TCTGTTGGGA TTCCTAAGCC CAGGATTACC 960
TGGGAGCTCC TGGGCTCACC ATGTGGAGAA ACTCTACCCG GAAAGAAGCC AACACTGAAG 1020
AAAGGAGAGC TTAAAGGGGA GGGGAGGGGG TAGGGGCATG AGGGAGAGAG ACGAACAGAT 1080
GGAGTCTTAA TGGCATCCTT TGAGTGCCGG GATCCAGCCA TGCCTAACAT CAGCTCTACC 1140
TCTAGGCTTT TCTGACACAT GAGCCAATAC ATTCTCTCTT GTTGAAGCTA TTTTGAGTCA 1200
GGTTTCTATC CCTTGTATAC AAAAGGGTTT TGATTAATTC ATTCACTCTA CAAATATGTA 1260
CTGAATGTTT TACTGTGGGC CAGGACTCAT CAGGCAATGT ACAGATGAAT GAAACAGTCC 1320
CCACCGTGAG CTGCTTCAAT GATAAGACTC TTCAGTGTGG AGCAAATAAA TGCACCAACT 1380
ATCTGCACCT CTTTACCTTC CAGGCATACG ATGAGTCAGT CCCCAGTCCC CTTGTGACTT 1440
GGGAGGCCAC GTGGCTACTT CTAACCCGGG AGGGGGAGAA GTGACGTGTG CCATTTCTGG 1500
GCCAGAGCCG TAACTGATGG TACAAGATCC TCCCCAAGGC CTCCCCTTCC TACTGGCGCA 1560
ACCCAGCAAT ATTCAAGATG GCGAACACCC TCTGGGACCA GGACGAGCAG AGCCACCACC 1620
AACTGCAATG CGCACGCAGC GAGAGTGAGA AATAAACCTT TTTATTTTAA GCTACCGAGA 1680
TCTGGAGATT ATTTGTTACC ATAGCAAATT CGACTAATAC CCTCTAAGAA CAGTAGCAGG 1740
GAAGGAAGGA ATCAGACAAC ACACAAGGAT ATAAAATAAA AGGTGGTGTC TGCAAAGGGC 1800
TGTGGGATGC 1810
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