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

TagContent
EnhancerAtlas ID
HS176-14682 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr16:2183670-2185470 
Target genes
Number: 56             
NameEnsembl ID
LA16cENSG00000261207
NME3ENSG00000103024
MRPS34ENSG00000074071
EME2ENSG00000197774
SPSB3ENSG00000162032
NUBP2ENSG00000095906
RP11ENSG00000261661
IGFALSENSG00000099769
FAHD1ENSG00000180185
HAGHENSG00000063854
C16orf73ENSG00000162039
HS3ST6ENSG00000162040
MSRB1ENSG00000198736
RPL3LENSG00000140986
NDUFB10ENSG00000140990
SNORA10ENSG00000206811
SNORA64ENSG00000207405
AC005363.9ENSG00000255513
RPS2ENSG00000140988
SNHG9ENSG00000255198
SNORA78ENSG00000238671
RNF151ENSG00000179580
TBL3ENSG00000183751
NOXO1ENSG00000196408
GFERENSG00000127554
SYNGR3ENSG00000127561
AC005606.14ENSG00000261790
AC005606.15ENSG00000260107
ZNF598ENSG00000167962
NPWENSG00000183971
SLC9A3R2ENSG00000065054
MIR1225ENSG00000221656
PKD1ENSG00000008710
RAB26ENSG00000167964
SNORD60ENSG00000206630
TRAF7ENSG00000131653
CASKIN1ENSG00000167971
MLST8ENSG00000167965
C16orf79ENSG00000182685
PGPENSG00000184207
E4F1ENSG00000167967
DNASE1L2ENSG00000167968
ECI1ENSG00000167969
AC009065.1ENSG00000167970
RNPS1ENSG00000205937
MIR940ENSG00000216095
ABCA17PENSG00000238098
ABCA3ENSG00000167972
CCNFENSG00000162063
C16orf59ENSG00000162062
NTN3ENSG00000162068
TBC1D24ENSG00000162065
ATP6V0CENSG00000185883
AMDHD2ENSG00000162066
CEMP1ENSG00000205923
PDPK1ENSG00000140992
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr16:2185222-2185233GCCCCGCCCCC+6.02
KLF5MA0599.1chr16:2185222-2185232GCCCCGCCCC+6.02
ZEB1MA0103.3chr16:2183721-2183732CCCACCTGCCC+6.14
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_48217chr16:2183604-2183906Psoas_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1621850342185366
Number: 1             
IDChromosomeStartEnd
GH16I002133chr1621836052183906
Enhancer Sequence
CCACCTTCCA GAACTCTCCC AGCGGCGGCC CCAGGTGTGT ACAGAACAGC ACCCACCTGC 60
CCACATGAGG TCACCCTGTG CCCTGTTGCA CACTTGGGGG GCCTGGCATT CGGAATCTTG 120
CCAGCTCAGG CTGGGACAGG CCACCAACTC CCAGGGTCCC CCTCCTCCAA ACCCCAGGAC 180
CAGAGCCTAA GAGGACAACA CAAGGCAGGG GCGGGGGCTC CACTGCTGTG CCAAGGGCCT 240
GGAGAACACG GGCCTTGCTC TCCGCTCAGC AGCCACCAGC GCCCTTCTCT CCCGGACAGC 300
TCCTGAGGGG CTGCTCTCAT GGACACCATC AGGTGCTGGG AAGCAGGAAC CACCAGGCCC 360
TGGACAGAGT CCCCAGTGAC CGGCCTGGCA GACAGAGGAG CCCTCAGCTA CAGCATCACA 420
AACAACGGGT GGGGTAGGTC TGATGCAATT CTGTGGGTGC TGTTGCCAGG CAGGAGGAGG 480
CCATCTCCAC AGAGACAGCC GCGAGACACA CGCGTCCGCA GTCAGGGAGC GCAGGAGCAA 540
TGTGGCCCCG AGGGGCACGG GCTCCATTGG TCCAGGAGAA CCCATTCTTC TCCCACCCTC 600
GAGACCACCC AGCAAAGCCC CAAGGACACA CGGCTCCCCT AAGGAAGGGT GGCCACAGGC 660
GGGAGTGACC CAGAAACGTT ACAAAACCAA ATGCCAGAAC CCACCCAATG TTTAGCAAGC 720
CTGGGGATGT GCCACGTCCC CCAGGGATCC AGCACGCACC CAAGGAGACA CTGTCCCGGC 780
GAGGAGCCTG GAGCCTGGGA AATACAAGGC ATCAGACTGG TCCCAAGACT CTCCCCAGCG 840
CTGGGGACAA CTGTCTGCTT ATCTTAGTCC CCTCCGCCCT TTTCAATCCA ACCCTGGGTC 900
CTGGGCACCT CATAGTTCCA AACCCCTGCT ATGCACATCC CGGCTGTGAT GCCTGGGACA 960
GGTCGTGTCA CCTCTCCAAA CCTGTTTCCT CATCTGTGAA ATGCAAATCT CCACGGTCCC 1020
TATGCCTCGG ATGGTCAGAG TCAGGATTCC GCATGACGAC CCCCAACAGG AGCCTGGCAC 1080
AGACCTGGCT CTGGGCAGCG TCTCCATAAA GGCCACCTGT TGTTTTTATC TCCCGAAAGC 1140
GAACATGACA AGGCTTTAAC CCCCCACGGC AATCCCCCCT CACCCCTGTT CTCAGGATAG 1200
CCTTGGAACC CAATAGCAGA GCGCCTGAGG CCCTTCATGA CCCCAGCCCA CCCGCGAGCC 1260
CACCTCCCAC CCTGCCCCTA CCCCTCACAC CTCCCGTGGC CAGCCTCCAG CCTCACGGTC 1320
TTTGCTCACA CCGTTCACCC CCCTTCTTCT GGACCCACCT CATCGCCCCT TCCTAAGCAT 1380
CAGCCCAATT CTTGCACATC CATCAAATCC TTTTCCAGAC ACCTCCTGGA ACTCTTCCCT 1440
GCCGCCCCCT ACAGCCATCC CCACCTCTCC GGGTACCCCG CAGCCCCAGG CCGCATCCCA 1500
ATTCCTCTCC AATTAGCGAC TGTTTGTCCT CCCAGCTGAG CGCGGCCTCC GCGCCCCGCC 1560
CCCGCTGGCG TCTGCAGAGC CCCCGGGTGG GACGTCTGTC TCCAGACCCG GGGTTTTTCG 1620
GCTCCCCGGG GCCGTGCCAA CCGCGGCTCC AGGCGTTCCT TATTTAGCAG GGCCGCCGTG 1680
CCGCGCCGGA GCCTCGCCCT GGGAGCGTCC TGGCCCGCGT CCTGCTTCCC GTCCCGGGCC 1740
AGGGAACGCG CCCACGCCCG CCCGTCCCGC GGCCTCTCCC GGGTGCCGCT GGGCCCGCTA 1800