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

TagContent
EnhancerAtlas ID
HS133-05987 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr11:66659060-66661630 
Target genes
Number: 49             
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
CARNS1ENSG00000172508
PPP1CAENSG00000172531
RPS6KB2ENSG00000175634
AP003419.16ENSG00000255949
PTPRCAPENSG00000213402
CORO1BENSG00000172725
TMEM134ENSG00000172663
AIPENSG00000110711
PITPNM1ENSG00000110697
CDK2AP2ENSG00000167797
NUDT8ENSG00000167799
RPL37P2ENSG00000239559
FAM86C2PENSG00000160172
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4008953chr1166660949hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:66661317-66661335TCCTCCTTCCTTCCTCAC-6.08
FOSMA0476.1chr11:66659829-66659840TGTGACTCATC+6.14
JUNDMA0491.1chr11:66659829-66659840TGTGACTCATC+6.14
Nr2f6(var.2)MA0728.1chr11:66660099-66660114GAGGTCAGGAGTTCA+6.22
Nr2f6(var.2)MA0728.1chr11:66659081-66659096TGAACTCCTGACCTC-6.22
Nr5a2MA0505.1chr11:66659674-66659689ACTGGCCTTGAACTA-6.5
ZNF263MA0528.1chr11:66659566-66659587GGAAGAGGAAGGGGAAGGAGT+6.22
ZNF263MA0528.1chr11:66660414-66660435AGGGGAGGCAGAGAAGGAAGA+6.64
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_00471chr11:66658889-66660128Adipose_Nuclei
SE_34512chr11:66658992-66660885HCT-116
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr116665941266660070
chr116666049566660764
chr116665973066659912
Number: 1             
IDChromosomeStartEnd
GH11I066891chr116665914366660981
Enhancer Sequence
CCACGTTGGT CAGGCTGGTC GTGAACTCCT GACCTCAGGT GATCCACCCA CCTCAGCCTC 60
CCAAAGTGCT GGGATTACAG GCGTGAGCCA CCGCACCCAG CCAATAGGCA AGTTTTTAAT 120
ATCAATATTG CCAAATAAGT CTCAAGGTAG TTATCCTAAT AATTTACACA GCCACTAGAA 180
ATACAACAGA ATGTCTATCT CCCCACATCT TTACCAACTG TTATATTGTT AGACTTTGAT 240
TTCTGTCAAC CTTGTAGTAT AAAATGGTAT CATTTTAATT TTCAGTCCCC TGATTATTAC 300
TGAAGTTGGC TATTTTCTTA TGATTGTGGA TATATTTTTA GGTTTTTCCT TTTGTGAACT 360
GCCTGTTCAC ATCATTTGCC CACTTTTCTG CTGGGCTGGT TGTCTTTTTC TTACTGAGCT 420
GTAATAAATC TTTATGTATT CTAGGCATGA ATCCATTCTC TGTTATACCC ATGGCAGACG 480
CTTGGGAGGA TGTTTAGCAA GTTATAGGAA GAGGAAGGGG AAGGAGTTGA GAGGGAATGA 540
CAAGTTGAAG AAGGAAGGAT GAGAATAAAA GGTGGGGCGA GTCCGGGAAC AAGGCTGCGA 600
GGCTCGGGTG AAAGACTGGC CTTGAACTAG ATGAAGAACA CTTCCCCTGA GACCAGAGTG 660
CCTAAGAGTT CTGGGACAGT CTCAGTTGTA AAACAGCCAG TGCTTGGCCA CAGGTGTCAC 720
CCAATACACT GACTCAGCCA GGGCCTGGGA TGACTAAGAG CTTTTTCAAT GTGACTCATC 780
AAGGCTGACA AGCACAGGCA TCACGTTCCA GAACGCACAA CCAAAAGGGC AAAGCAACAG 840
TCCAGGCAGG TCAGCCTGTA GAGACAAGAC TTCCTACTGA CATCCAAGCT ACTCGTTTGC 900
CACAGCTGCT CCAAGGATGG CAATAATGAG TGCGAGCTGC ATCAGAGATG AGAGATTGAA 960
CTTTAAGAAA AATGTCGCCG GGCGCGGTGG CTCACGCCTG TAGTCCCAGC ACTTTGGGAG 1020
GCCAAGGTGG GTGGATCATG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA GATGGTGAAA 1080
CCCCGTCTCT ACTAAAAATA CAAAAAAATT AGCCAGGCAC GGTGGCGGGC GCCTATAATC 1140
CCAGCTTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC GCTTGAACCC AGGACGTGGA 1200
GGTTGCAGTG AGCCAAGATG GCGCCACTGC ATTCTAGCCT GGGTGACAGA GCAAGACTCC 1260
ATCTCAAAAA AAAAAAAATT GTTGGCTTTT AGTATTAACT GTGAGTGTTT GGTATTCATG 1320
TTGGATCTGC TGCTGATGAT GTGGGGGTGG GTGGAGGGGA GGCAGAGAAG GAAGAATTAG 1380
AAGGCCACAG AAGCCCAGGT TGAAGGGCTG GGGCTGCTGC AGTGGAAATA TCTTTTAAGA 1440
TGCTACTTGG CAAGCATGAT TCAACCCTGA CAGACCCTTA GAACAAGTCA GACGACCTGA 1500
AAGATGAGAT TCTGCTGTCC AGCTGCACCG TGTCAGTGAG GACCCCCACT GTGACCCCAG 1560
GGCACGACTC ACTCCCACGG GCTTGCCTGA CTCCAGCTCT GTGCTATGAC ATCACGTTGG 1620
TAGCCTGACA CGGGCCACAG TGGGCATATT TATGCCACAG AAATTGGCAA ACACTATAAT 1680
CAAGGCCCTT TCCTCACTTC CCTAAGAGCC ACTCCTGACA GAGCAGTGGG TGGCATGCAA 1740
ATCCCAGAAG GGCCCAGAGA CGGGGAGTGA GGGGAGCAGC GTAGACAGAG TCGCTTCTCC 1800
ACTCTCCCTT TTGCCTACAG AACCCAAATA AAGAAGGCTC TTTTCTTTTT TACAGACCTG 1860
GTGTCCAAGT ACTTAATTTG ATCAAAACAT GAGGATGAGC TAAGGAAGAC AGCAGACAGG 1920
CACTCTATCA ATGTCTTAAG GTAGTTCCAA TGACATTCTG CAACATGAAT TAATCTTTGA 1980
GGATATCAAC ATAAAAATTC TTTTGAGAAT CTCATTTAAC AACTGGAAAA TTATTCTTTT 2040
GTCTTCTAAG GGACTGATTT CTTTACCCCT GCTCTCAACA CCTTCTTTCT CTCTCTCCAT 2100
CAACACAGGC ACTTGGAGGT TGAAGCGTGG GGGTGTAAAA TCACGCTTTT TGGTGGACAT 2160
GGCAAATGCC TATTCTATAG CAGAACTTAG CCCCCGCCCC CTACCCCCTC ACTCCCCCTC 2220
CCAAACTGCA CACATACACC AAACCCAACC AGACACCTCC TCCTTCCTTC CTCACCACCC 2280
TCTCCCTGGT CACCAAGGGT TAAGCTTAGG GTCTTCTTTA GCTCTTCCCC TCCCTCACCT 2340
ACCATCTGGT CAAGAAGTCT GGGCAGTTTT ACCTCTTTAA TCCCTCACAT CCTTCCCTCT 2400
TTTCATTTCT AAGAAGAGGA CCCTGAAATG TCCTCTTCTT ACTACTTAAC TATCGTAAAA 2460
ACCTCCTACT CATTACCACA GCTCTAGCTA CCAATCCACA TTAGGTACTA GGGATAGCTA 2520
GCATCCCCAA ATACAGGCAT GACGGCACTC TTCCTGAAAA GTGGGGTAAT 2570