EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-16020 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr16:2472770-2474400 
Target genes
Number: 44             
NameEnsembl ID
MRPS34ENSG00000074071
NUBP2ENSG00000095906
FAHD1ENSG00000180185
HAGHENSG00000063854
MSRB1ENSG00000198736
NDUFB10ENSG00000140990
RPS2ENSG00000140988
GFERENSG00000127554
SYNGR3ENSG00000127561
AC005606.14ENSG00000261790
AC005606.15ENSG00000260107
ZNF598ENSG00000167962
NPWENSG00000183971
SLC9A3R2ENSG00000065054
TSC2ENSG00000103197
NTHL1ENSG00000065057
RP11ENSG00000259933
PKD1ENSG00000008710
RAB26ENSG00000167964
TRAF7ENSG00000131653
MLST8ENSG00000167965
PGPENSG00000184207
ECI1ENSG00000167969
AC009065.1ENSG00000167970
AC009065.2ENSG00000207715
CCNFENSG00000162063
C16orf59ENSG00000162062
NTN3ENSG00000162068
TBC1D24ENSG00000162065
ATP6V0CENSG00000185883
AMDHD2ENSG00000162066
CEMP1ENSG00000205923
PDPK1ENSG00000140992
CTDENSG00000261093
AC141586.5ENSG00000215154
PDPK2ENSG00000205918
KCTD5ENSG00000167977
SRRM2ENSG00000167978
TCEB2ENSG00000103363
ZG16BENSG00000162078
TNFRSF12AENSG00000006327
THOC6ENSG00000131652
IL32ENSG00000008517
U1ENSG00000252561
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1624729232473140
Number: 1             
IDChromosomeStartEnd
GH16I002423chr1624732012473370
Enhancer Sequence
GAGATCTGGG GCTTCCTTCA GGCCCTCCAC CTCCAGTTAC AAGATAAGTT CCAGTTCTTC 60
CCAGACCTGG AGAGCAGGGC AAAGCCCCCA GCTCTGGGCA TGAGGTCACT GCGCAGGTGG 120
TTGGGGGCGG CCTGCAGGAA GAGGTAAGTG GCCTGGGCTG CCTCAAGGCA CCCCTTCCTC 180
TTGGTCCTGG GCTTGACTGG ATTATGAAGC TGACCCAGGC CAAAGGCAGC TTACGTGGCT 240
GAGGTCAGGC AGATGGCACC ACAGGTGTTA CTGTCCTGAT AAGGTGAGGA CGGACCTTTC 300
TCCCTGCCAC TTTATGAAGG GCTATTTTCA GTAAGTTTGC ATTTTAAGCC CAGAGTTACC 360
TCATACCACT GGGTCTGCGG TACTTGAACT ACTGATGTTC TGCTAAGGCG CATGGGGTAT 420
TTCTCAGGCT TCTGTTGTCA GTGATAGAAG CCCGACTCCA ATTAAAGCAA GGCCACAGGC 480
CCCGCAGGTC CAAGGACTCC CTTCGTGTTG TGTGCAGCGC CCCCGGAGGC ACACAGCGGT 540
ACTGCACACC CAGGATTGGG AGGTAGAGGT GCCCACGCCT CTAGCAAAGT GAGCCCGGGG 600
TCAGATGATG ATGTCCCTTG GGTCTTCTCT CTTTGGTGGC TCCTGTTTCA AGCAGGTTTT 660
TACGTTTCCC TGCATCTTCT GAAGATCAAA TGAGTTCACA TTTGCGAAGT TTAGAACAGT 720
GTGTTGCACA TAGTAAATGC TATATGGTTT TTTTGTTTGG TTTTGTTTTT TAGAGTTTTC 780
ACTCTTGTTG CCCAGGCTGA AATGCAATGG CATGATCTCA GCTCACTGCA ACCTCTGCCT 840
CATGGGTTCA AGTAATTCTC CTGCCTCAGC CTCCCGAGTA GCTGGGATTA CAGGTGCCCA 900
CCAACACGGC CAGCTAATTT TTGTATTTTT AGTAGAGACA GGGTTTCACC ATGTTGGCCA 960
GGCTGGTCTC AAACTCCTGA CTTCAGGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG 1020
GATTACAGGT GTGAGCCACC ATGCCCATCC AGTTTTTTTT TTTTAAGTTA GCTAAGATGG 1080
GCCAATGCCT TTCCTCTCAG ATGGAGAGGT GCTTGCCCTC AACACTTCAA ACCCTCAAAG 1140
AAGACTCGTC GGCCGTGTGC TCACCCTGGA CTCATCCCTG TGTCCAGGGG AACAAGTTAT 1200
TTCCTGAGTG GATAGCCCAA GCCACAATTC AGCTCTGGGT GAAAGTGGTG GACTGCATTG 1260
CTGAAAGCCC CATGAGGGGT GTGGGAATAC TTCCTGAATA GAGAAGGAAA GGGGGTGAGT 1320
GTTGAGCCGG CAGTGCTCAC TGCTGGAGAC TGACCATTGC CGTCACCCAA CCTTCTCCCT 1380
TCCACCCCCG GTGGTGGTAA CAAGCCGAAG TTGAGCACTG GCATTGATCG CCCTGATTGG 1440
AGAGCCTGCC TTCATCTTCC TGGATGAGCC ATCCACTGGC ATGGACCCCG TGGCCCGGCG 1500
CCTGTTCTGG AATGCTGTGG CACACGCCCA CGAGTCTGGC AAGGCCATCA TCATCACCTC 1560
CCATAGGTAG AGCCTGGGTC TGTGGGTCAC TGGAAGTTTC AAAACCAGGT AGGCTGGGAA 1620
GAAGCCAGGT 1630