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

TagContent
EnhancerAtlas ID
HS105-29441 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr16:2022210-2024000 
Target genes
Number: 49             
NameEnsembl ID
IFT140ENSG00000187535
CRAMP1LENSG00000007545
HN1LENSG00000206053
MAPK8IP3ENSG00000138834
LA16cENSG00000261207
NME3ENSG00000103024
MRPS34ENSG00000074071
EME2ENSG00000197774
SPSB3ENSG00000162032
NUBP2ENSG00000095906
RP11ENSG00000261661
FAHD1ENSG00000180185
HAGHENSG00000063854
C16orf73ENSG00000162039
MSRB1ENSG00000198736
RPL3LENSG00000140986
NDUFB10ENSG00000140990
SNORA10ENSG00000206811
SNORA64ENSG00000207405
AC005363.9ENSG00000255513
RPS2ENSG00000140988
SNHG9ENSG00000255198
RNF151ENSG00000179580
TBL3ENSG00000183751
NOXO1ENSG00000196408
GFERENSG00000127554
SYNGR3ENSG00000127561
AC005606.14ENSG00000261790
AC005606.15ENSG00000260107
ZNF598ENSG00000167962
NPWENSG00000183971
SLC9A3R2ENSG00000065054
TSC2ENSG00000103197
NTHL1ENSG00000065057
PKD1ENSG00000008710
RAB26ENSG00000167964
TRAF7ENSG00000131653
CASKIN1ENSG00000167971
MLST8ENSG00000167965
C16orf79ENSG00000182685
PGPENSG00000184207
E4F1ENSG00000167967
DNASE1L2ENSG00000167968
ECI1ENSG00000167969
AC009065.1ENSG00000167970
RNPS1ENSG00000205937
ABCA17PENSG00000238098
ABCA3ENSG00000167972
ATP6V0CENSG00000185883
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr16:2023528-2023549GGTGGAGGCAGTGGAGAAGGA+6.26
ZNF263MA0528.1chr16:2023540-2023561GGAGAAGGAAGGAGAAGGGGC+6.54
Number of super-enhancer constituents: 13             
IDCoordinateTissue/cell
SE_68103chr16:2008747-2090503TC32
SE_68104chr16:2008747-2090503TC32
SE_68105chr16:2008747-2090503TC32
SE_68106chr16:2008747-2090503TC32
SE_68107chr16:2008747-2090503TC32
SE_68108chr16:2008747-2090503TC32
SE_68109chr16:2008747-2090503TC32
SE_68110chr16:2008747-2090503TC32
SE_68111chr16:2008747-2090503TC32
SE_68112chr16:2008747-2090503TC32
SE_68113chr16:2008747-2090503TC32
SE_68114chr16:2008747-2090503TC32
SE_68115chr16:2008747-2090503TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1620236902023740
Enhancer Sequence
GCCCGGAGCT CTGGGGCCGT GCGGGGAGGG AGCTGGGTTT GCAGCCGGCA TAGCGGAGGC 60
GCGCGTGGGG TGGGCACGCA TTGGGGTCCG TGGAGGCGAG AGGCTGTGTG TGCGCCGGCC 120
CGCGGGGTCG CGGAGGCTGC GGTGATACTA GGCGGGAGAG CCGGCCCCGG CTGCTCTCGG 180
GGAGGACGGC GATCGGAGCC CGGCCGCCGG GAGCAGCAGC GTGGGCTCAT CGAGAAGCCG 240
GCTATGGGGT GGAGTGGGGA CCAGAAGTCC CGATGAGGGG AGGAGAGGGC TGAGCCTAGG 300
TCGGGGCTGG TCCCGGGAGG CGGCGGGGGC GAAGAACCAC CTCTGAGCAG TCGGCCTGGG 360
GACCTTTCAT CCGCGATCCG TCTTCTCCAG GGAGCAGGGA GAATGCAGGA GAGGGGCGGG 420
TCCGCAGAAG CCCAGGAGGC CCTGAGTGCT GTGCCCCGTC ACTCCCCAAG CCTTTGCCGA 480
ACAGCAGTGC TGGTGCCCCC GCCCTGGCAG CGCAGCCTCA TGGGATTATC GTTTCCACTG 540
GCGGCTGTGG GGCTTTGGTT GTGCCAAGCA CTGGTAAAGG AAAGTCCCAG GCTGGCAGCA 600
CCGTCGTGGG AGGGTCAACT GGGTGCGGGG GCTGAGGGGC CGCTTTCGTT TTGGCAGTCA 660
GGCTTCCAGA AGCGCAGTGA GCCAGGCCTT GACATCTGGG AAGAGAAGCC CAGGCCGCGT 720
ACAGGGAATA GGGGGAAGAT AGGAAACCCG TCCCAGAGGC TGGGACAGGA GCAGTGGGGT 780
GCACTGTGGG CCATGAGAAG GAAAGAAAGC AGAGGCAAGG GTGGCAGAGG CTCTTCTGGG 840
CAAGGTCTGG GAGGTGTGTG GGCAGAAGGG AGGGGCTAAC GCAGGGCAGT GACATCTTCA 900
GTTATGTTCT GAAAGGTACC TGGCAGCAGG GTTAAGAGGT AGGTAGGGGA GGCCGGGCGC 960
GGTGGCTCAC GCCTGTAATC CCAGCGCTTT TGGAGGCCGA AGCGGGCGGA TCACGAGGTC 1020
AGGAGATTGA GACCACGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAA TTAGCTGGGC 1080
GCAGTGGCGG GCACCTGTAG TCCCAGCTAC TCGGAGAGGC TGAGGCAGGA GAATGGCGTG 1140
AACCCGGGAG GTGGAGCTTG CAGTGAGCTG AGATCGTGCC ACTGCACTCC AGCCTGGGCT 1200
GGAGACCCCT TCTCAGATCG AGACCCCTTC TCAAAAAATA AATAAGTAAA AAGAGGTAGG 1260
TAGGGGGTCC AGTGAAGAGG CCAGAGTGGC TGGCCAGAGA CTGTGATGGG CTGGACCAGG 1320
TGGAGGCAGT GGAGAAGGAA GGAGAAGGGG CACGAGTGAG GTCACAGAAA TGACAGCTGC 1380
TCGTGGGACC CGGGCTCTGG GCAAGCCTGG GGATGGAGAG AGGAGTCAGG GAGGGGAAGA 1440
GGTATGCCAG ACCTCAGGGA TGAAGACACT GGGAGGATGT GCTCTGGGCT GGCTACCCAG 1500
GCCTGGCCAC CCACCGCCGG CAGGGGTGTT CCCAAGGAGC CCCCTGGCTC TCACTGGGGA 1560
ATCCCTGGAA GCCCTGGGCT GTTGGGCTGA CTCCACCTGA CACAGGCCCA CCCCCTACTG 1620
CCTCAGGGAT CACCAGCCAG CTGCGGGTCT CTACTTCTCA GTGACGACGG TAGCTACAGC 1680
CCCCTGCAGT ACTGCTGGTT CCACCCCATG CCCTGTCCCT GCTGTTGCCC AGAAACTCAA 1740
GGGCAGGGGC CATTGGGGTC ACTTGGAGAG GAGCACCTAG CACAGGGCGG 1790