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

TagContent
EnhancerAtlas ID
HS105-29453 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr16:2089030-2089810 
Target genes
Number: 49             
NameEnsembl ID
IFT140ENSG00000187535
CRAMP1LENSG00000007545
MAPK8IP3ENSG00000138834
NME3ENSG00000103024
MRPS34ENSG00000074071
EME2ENSG00000197774
SPSB3ENSG00000162032
NUBP2ENSG00000095906
FAHD1ENSG00000180185
HAGHENSG00000063854
LA16cENSG00000260541
C16orf73ENSG00000162039
MSRB1ENSG00000198736
RPL3LENSG00000140986
NDUFB10ENSG00000140990
SNORA10ENSG00000206811
SNORA64ENSG00000207405
AC005363.9ENSG00000255513
RPS2ENSG00000140988
SNHG9ENSG00000255198
RNF151ENSG00000179580
TBL3ENSG00000183751
NOXO1ENSG00000196408
GFERENSG00000127554
SYNGR3ENSG00000127561
AC005606.14ENSG00000261790
AC005606.15ENSG00000260107
ZNF598ENSG00000167962
NPWENSG00000183971
SLC9A3R2ENSG00000065054
TSC2ENSG00000103197
NTHL1ENSG00000065057
RP11ENSG00000259933
PKD1ENSG00000008710
RAB26ENSG00000167964
TRAF7ENSG00000131653
CASKIN1ENSG00000167971
MLST8ENSG00000167965
C16orf79ENSG00000182685
PGPENSG00000184207
E4F1ENSG00000167967
DNASE1L2ENSG00000167968
ECI1ENSG00000167969
AC009065.1ENSG00000167970
RNPS1ENSG00000205937
CCNFENSG00000162063
C16orf59ENSG00000162062
NTN3ENSG00000162068
ATP6V0CENSG00000185883
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZIC1MA0696.1chr16:2089208-2089222GACCCCCTGCTGTG+8.12
ZIC3MA0697.1chr16:2089208-2089223GACCCCCTGCTGTGT+7.66
ZIC4MA0751.1chr16:2089208-2089223GACCCCCTGCTGTGT+7.61
Number of super-enhancer constituents: 21             
IDCoordinateTissue/cell
SE_01523chr16:2088440-2090153Adrenal_Gland
SE_02985chr16:2084697-2089730Bladder
SE_32284chr16:2084750-2091771Gastric
SE_41007chr16:2082164-2091659Left_Ventricle
SE_42469chr16:2074866-2091667Lung
SE_46742chr16:2088442-2091458Ovary
SE_58160chr16:2089020-2089625VACO_9m
SE_58160chr16:2089653-2090595VACO_9m
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
chr1620890392089354
Enhancer Sequence
ACACGCCTCT GTCTTTTCTG AGCCTCCTCC CCGTGGGGTG AGAGGGGTGG AGGGATGAGG 60
CTGTTTCAGG GAGCCCCCTC CCCGAGTCTC AGCAGCTGGA AACGGTCTCG TTCCTGAGCC 120
CGTGCCCTGC ATCCATCTGC TCCCAGCCCT GCTCCATCTC CCCCGCTGAC CCCCATGGGA 180
CCCCCTGCTG TGTGGCACAT CCTGGGCCCA TGCCCATCTC TCTTATTTGG CAGACTCAGC 240
CTCCCACCTT CACCTTCCCT GTGAAGCCAT CCGGCCCCAC ACAACACCCA CACGGGCCAC 300
CCTTTGCCCA ATTCACCCTG CGACCTCTAG CAGTCACAGG TCAAGCTTTG TACCCTGTGG 360
CGCCCTGCCT GGGTCCCCAG TGTCCCTTTC AAGGCCGGGT AGCTCTGTAA ACAGGGGTGG 420
GACCCTGGCA GAGGCTGGGC TTTGAGGGCA TGAAAGTTCA GGAGCTGGCG GTGTCCGGGC 480
TGGGAAGCTG GGGGGCCGGC GGTGGATAGC ATGAGGGGCC AGGGTCCCCA GCCAGCTGCC 540
CGGGGGCTGC TTGCTTCCCC AGCGGACTTC CAACAGCTGG CTGCAGCTGG CTCTCCCCAC 600
TTCCTCCCTC CCAGGTTCAT GCACACCCCC TCCCCCTCCC TGAGTACATA GCAAAGATTG 660
TCACGTCCCC AGCCGGCCTC CCAGGCAGCC CTGCTCCAGA CACGCGAGCA CGGGTGTGTA 720
CGAACACATC CTTGTATGCG ATTCCCAGGC TCTCTGCCCC CTCAGGGACA GACATCAGCC 780