EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-29465 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr16:2154640-2155320 
Target genes
Number: 52             
NameEnsembl ID
CLCN7ENSG00000103249
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
C16orf59ENSG00000162062
TBC1D24ENSG00000162065
ATP6V0CENSG00000185883
AMDHD2ENSG00000162066
CEMP1ENSG00000205923
PDPK1ENSG00000140992
SRRM2ENSG00000167978
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr16:2154892-2154913AGGGGAGAGAGGAGAGGGGAG+6.12
ZNF263MA0528.1chr16:2154922-2154943AGGGGAGGGGAGGAGGGGAAG+6.17
ZNF263MA0528.1chr16:2154970-2154991AGGGGAGGGGAGGAGGGGAAG+6.17
ZNF263MA0528.1chr16:2155020-2155041AGGGGAGGGAAGGGGGAGGGG+6.47
ZNF263MA0528.1chr16:2154899-2154920AGAGGAGAGGGGAGTGGAGAA+6.4
ZNF263MA0528.1chr16:2155041-2155062AGGGGAGGGGAGAGTGGAGGG+6.51
ZNF263MA0528.1chr16:2154995-2155016AGGGGAGGGGAGGAGGGGAGG+6.61
ZNF263MA0528.1chr16:2155024-2155045GAGGGAAGGGGGAGGGGAGGG+7.01
ZNF263MA0528.1chr16:2155031-2155052GGGGGAGGGGAGGGGAGGGGA+7.81
ZNF263MA0528.1chr16:2154887-2154908GGAGGAGGGGAGAGAGGAGAG+8.74
ZNF263MA0528.1chr16:2154884-2154905GGAGGAGGAGGGGAGAGAGGA+9.59
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1621552782155318
Enhancer Sequence
CCCCTGTGTG GAGCCAGCAG TGTCCAGCCC CGCTCCTGGC CCCACTCCTT GCACACGCCC 60
TCCTCTCTAC ACGGGTCCTC ACCTGGCTCC CACCCCCAGC CCTGCAGCTG GAGAGCCCAC 120
TTGACTGGAC CCCCACAGCC TCCTCACTAA GCATTTTCTG TGGCTCTGCA TGACCCAGGG 180
CCTCCACCTG GGGACCACGT GATGCAGCCC ACCGACCACA CAAGGCACCT CTTCACATGA 240
GAGCGGAGGA GGAGGGGAGA GAGGAGAGGG GAGTGGAGAA AAAGGGGAGG GGAGGAGGGG 300
AAGGGCTGGG GGGGAAGAAG GGAAAGGGCT AGGGGAGGGG AGGAGGGGAA GGGCTAGGGG 360
AGGGGAGGAG GGGAGGGGCT AGGGGAGGGA AGGGGGAGGG GAGGGGAGGG GAGAGTGGAG 420
GGCACAGAGC AGCATCTTCT TAGTCCCTCC CCACATCTGG GCCCCTCTTT ACACCCTGGG 480
TCCCCCGAGA GGCACCCTGC GTTCACACAG GACAGAACGG CTGAGGCTAC TGAAGCAGGT 540
CAGAGACCGA GGAACGCCAT GGCAGGAAGG AGCCCAGGCT GGAGGCTCAG CTCCTCGGCC 600
AAGCTGCCCG TCTGCCCTGG GGGGCTGAAC CCAGTGCCCT GGCAGGCATG CGGGGCAGGG 660
TGAGCAGGTG GGGCCATCCT 680