EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS133-05985 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr11:66641730-66644920 
Target genes
Number: 48             
NameEnsembl ID
RP11ENSG00000255320
KLC2ENSG00000174996
RAB1BENSG00000174903
CNIH2ENSG00000174871
YIF1AENSG00000174851
CD248ENSG00000174807
RIN1ENSG00000174791
BRMS1ENSG00000174744
B3GNT1ENSG00000174684
MRPL11ENSG00000174547
PELI3ENSG00000174516
DPP3ENSG00000254986
CTDENSG00000255517
BBS1ENSG00000174483
ZDHHC24ENSG00000174165
ACTN3ENSG00000248746
CTSFENSG00000174080
CCSENSG00000173992
CCDC87ENSG00000182791
RBM14ENSG00000239306
RBM4ENSG00000173933
RBM4BENSG00000173914
SPTBN2ENSG00000173898
C11orf80ENSG00000173715
RCE1ENSG00000173653
LRFN4ENSG00000173621
PCENSG00000173599
SYT12ENSG00000173227
RHODENSG00000173156
KDM2AENSG00000173120
ADRBK1ENSG00000173020
ANKRD13DENSG00000172932
SSH3ENSG00000172830
POLD4ENSG00000175482
CLCF1ENSG00000175505
RAD9AENSG00000172613
PPP1CAENSG00000172531
RPS6KB2ENSG00000175634
AP003419.16ENSG00000255949
PTPRCAPENSG00000213402
CORO1BENSG00000172725
TMEM134ENSG00000172663
AIPENSG00000110711
PITPNM1ENSG00000110697
CDK2AP2ENSG00000167797
NUDT8ENSG00000167799
RPL37P2ENSG00000239559
FAM86C2PENSG00000160172
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs79214621chr1166642403hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr11:66642270-66642281GAAGATAAGAA-6.02
NKX2-5MA0063.2chr11:66641789-66641799CTCAAGTGGT-6.02
Nr2f6(var.2)MA0728.1chr11:66641777-66641792TGAACTCCTGACCTC-6.22
Stat6MA0520.1chr11:66642450-66642465AGTTCTCAGGAAGAA-6.93
ZNF263MA0528.1chr11:66642060-66642081AGAAGAGGAGGAGGAGGAAAG+6.73
ZfxMA0146.2chr11:66641802-66641816CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_00471chr11:66641441-66647963Adipose_Nuclei
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116664237466642420
chr116664443466644547
Enhancer Sequence
GTATTTTAAA TAAAGATGGG GTTTCACCAT GTTGGCCAGG CTGGTCTTGA ACTCCTGACC 60
TCAAGTGGTC TACCCGCCTC GGCCTCACAA AGTGCTAGCA TTACAGGTGT GAGCCACCAC 120
ACCCGGCCGA TCTGATTCAT TTCTTAGAAA ACGTTTAAAA CACTTGACTC AGCCATTTTG 180
TTTTAAGTAA GGAACATAAA AACATACTCA AGAAATGAAA CAAATATTGC AAAAACCTTA 240
GTGCCATATT ACAGCCAACA ACCTAGAAAA GGGGAAATAA AGACAGAAGA AAAAGAAAAG 300
AGAAGAAACA AGGAAATAAG TAGAAGAAAG AGAAGAGGAG GAGGAGGAAA GACCCACAGC 360
CAGGGGAGAA AAACAGAAAA CCCCACTAGG GGCAGACCTT ATGCCAGGCA CAGTTCTAAG 420
CCTTAGGAGT CGAGAACACA ACAGTGAAGG GTTCTGCTCA TGGAAGATGA ATGGCAGTGA 480
AAGGAGCAAA GAAAAGAAAA ACAAGACACA AATCAGAACA TTTCAGATCA CAAGTGCCTG 540
GAAGATAAGA AACAGGTGAC ATTTTGCGAA TGATCTGGGG CGGGTGCAGG GGTTTGGGGG 600
CTGGATATTA GAAAAGGCCT CTCTGAGGAG GGGACACAGA AGCTGGGACC TGGATGGGGA 660
GAAGTCGGCC ACGCACAGAT CCGCAGAGAA AGCTCCAGGA AGAAGGGATA GCAATTGTGA 720
AGTTCTCAGG AAGAACAGGC TTGGTGCTGT CCTGAGAGAG GGAAGTGTGA GCCCACGGCC 780
TGAGGTGGGG CTGCAGCCAC AGACAGGGCC CAGTGGTTGA GGCCTCCCTT CAGCCATGGA 840
CAGGACAGGA GGGACATGAT CGATGCACAG TGGAAAGGAT CTCTCTGGAC TGGCGAGCAG 900
CAGGGGCTGA CAGACGACGC ATGTCTGGGG CAATTCAGAG GCTGAGCTGA GAGACGCGGA 960
GCCTCTGACA GGGGGAAGCT ATGGGGGTCG GGGTGGGGCT TAGGAAACAT CTGGGCTATG 1020
ACAGACAAGA TTCGTCGAGA GACCCCCCAT AGAAAGCAAG GTAGAGGAAG AAATCCTGTA 1080
TGGGTGGGTG GAGATGACTT TTCCTGCTAT AAGAAGGGCA AGACAGAAAA GGCAGGGCTG 1140
GGAGTGAGGC AAGCTCACAG AGGGGGAAGA GCAGGGACAA GAACCTGGGC AGCATCACAG 1200
GGGCGGTGGT GTCTGAAGCC AGGGAGAGAA CAGCCTGGGA GAAGTGGGTC AGGCCTGCGT 1260
CTTCAGGCCC ACTGGAGTTG AGTCTGGCCG AGGAGGAAGA GCCAAGAAGG AGCCCAGGGG 1320
GGATGCCTGG AGGAGGGAGG GACGCACGGG TCGCTGGGCA GAAGCGAGCG GCTCTCAGGA 1380
GGATGGGGCG CGAGTTGGGC AGAGCATGAC TCCCAGAGGC AGGGTAAGAT GGGGGCTGGG 1440
AAGGGGCCAC TGCGGTGACC AGGAGGCACC CAGGTCACAC CCGGCTATGG TGAACGTGGG 1500
TAGAGTAACC TTGCTGGACT CTGGGCTCCT CCTCTTTCTA AAATATACCT TGTCCTTATT 1560
CATTGCACAG TGGAGAAACC TGGCGGACAC CACGCTGACC GAGAGATGAA GGTTAATATC 1620
ACTAGCACCG AAGGGATACC ACACACCTCC TGATGGGGTT CCCGCTGCCG TGCACGGCCT 1680
GAATTTAATC AGGAGAAAGC AAGGGGCAAA CTCAAATTCA GGGAAATTCC ACAGAATAAC 1740
TGGCTTGGAC TCTTCAAACA TGTCAAAGGT CGTGAGAGAC AAAGACGCAA GAACGGTTTC 1800
AGATGAAAGG AGACCAAAGC AACAATGGTG AGAGCCACAC ACGATCCTGG ATTGGATCCG 1860
GGTTTCTATT GCTAAGAGGA CATCAGGGGA CAACGATACA ATTTAAATAA GGTCTGCAGG 1920
TTTGAAAGAG GATTGCGTTG ATATCAATTT CCTGATCTTG ATCAGTGGAC TGTGGTTATG 1980
TTAGAGAACA GCCTCATTCT TAGGGAAAAA CACTGAGGAA CTCAAGGGTC CACGAGCACC 2040
ACATCTGCAA TTTACACCCA CTCACATGGT TCAGGGAAAA ACGGGAACAA TGAAGCAAAT 2100
GCTAGTATTG GGGGAACTGG GGTCAGGGGT ACGAGAATTC TTTGTCTTAC TCTTGCAACT 2160
TTACTGAAAG TCTGAAATCA TTTCAAATTG ACAAGTGAAA AGAACCATAC CCACCGCTAA 2220
TGCCGCTGGA GGAGATAACC TTAGGGAGTG CATGCCCCAG CACCTGCTGC TCAAGAGGTG 2280
CCGGGAGCAC CAGCGAGGAG CTCAGGTGTG GAGACACCCT GCTCAGAGCA GGATGAACGT 2340
CAGACGTTAT CACCCTGCTA TCTCCCACAT GCAGATCTAC AATCCTCTAA GCCCTGCTCC 2400
AGGCGAGTTA TCGGATGCTG CCCACTAGGA GGACAGGTCT TTCCCAGCTG GGAGCAGGCG 2460
GCACTGGCAT CAGAGAGCAG GTGTGGGGTG TAAATCTCAC CCTCCTCCTG GGCACCAAAT 2520
GTCTACTCTG CTGAGCGCTG GGAAAGGCCA TGTCAAAAGA GCTCAAGTTA CCACATAGGG 2580
CAAAGTCAGG AAGAGGCGAG GGGAGCCTTC GGGACAAGCA CAGCAACAAG ACAGCAAACA 2640
CAAGTGGCTC TTGAACCCAC GAGAAAGCAA GAGATTCAAA ATACAACCAT GAGGTGCCAC 2700
TCCTGCCTGG GAGCTTTGTA AATGCAGTGC TGAGCGCCAG GAAGGCCTTC AGGAGGCGGC 2760
CCGCAGGCAC TGCTGAGCAT CACGGCAGCT TCTCCGGGAA GCTGTTTGCA AAACTTATCA 2820
AGAGCCTTTA AGGTATTTAT GCCCGGCCAG GCGCGGTGGC TCACGCCTGT AATCCCAGCA 2880
CTTTGGGACG CTGAGACAGG CGGATCATTT GAGGTCACGA ATTCAAAACC ACCCTGGCCA 2940
ACATGGTGAA TCCCCGTCTC TACTAAAAGT ACAAAAATTA GCCCAGCATG ATAGTGGGCG 3000
CCTATAGTCC CAGCTACTCG GGAGGCTGAG GCAGGAGAGT TGCTTGAGCC TGTGAGGCGG 3060
AAGTTGCAGT GAGCCGAGAT CGCGCCATTG CATTCCAGCC TGGGTGATAG AGCGAGACTC 3120
CATCTCAAAA ACAAAACAAA ACAAAAAAAG CCGGGCACAG TGGCTGACGC CTGTAATCCC 3180
AACACTTTGG 3190