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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-17030
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr16:30544470-30545510
Target genes
Number: 60
Name
Ensembl ID
AC009133.19
ENSG00000262323
MAZ
ENSG00000103495
AC009133.15
ENSG00000259952
CDIPT
ENSG00000103502
SEZ6L2
ENSG00000174938
ASPHD1
ENSG00000174939
CTD
ENSG00000247735
TMEM219
ENSG00000149932
TAOK2
ENSG00000149930
INO80E
ENSG00000169592
HIRIP3
ENSG00000149929
ALDOA
ENSG00000149925
PPP4C
ENSG00000149923
YPEL3
ENSG00000090238
GDPD3
ENSG00000102886
MAPK3
ENSG00000102882
RP11
ENSG00000261416
BOLA2B
ENSG00000169627
CD2BP2
ENSG00000169217
TBC1D10B
ENSG00000169221
ZNF48
ENSG00000180035
SEPT1
ENSG00000180096
DCTPP1
ENSG00000179958
SEPHS2
ENSG00000179918
ITGAL
ENSG00000005844
ZNF768
ENSG00000169957
AC002310.12
ENSG00000235560
AC002310.11
ENSG00000261459
ZNF747
ENSG00000169955
AC002310.10
ENSG00000260494
AC002310.13
ENSG00000260869
ZNF764
ENSG00000169951
AC002310.7
ENSG00000239791
ZNF688
ENSG00000229809
ZNF785
ENSG00000197162
AC002310.17
ENSG00000261588
ZNF689
ENSG00000156853
PRR14
ENSG00000156858
FBRS
ENSG00000156860
SRCAP
ENSG00000080603
SNORA30
ENSG00000206755
PHKG2
ENSG00000156873
RNF40
ENSG00000103549
C16orf93
ENSG00000196118
ZNF629
ENSG00000102870
MIR762
ENSG00000211591
BCL7C
ENSG00000099385
AC106782.20
ENSG00000262721
CTF1
ENSG00000150281
FBXL19
ENSG00000099364
AC135048.13
ENSG00000261487
ORAI3
ENSG00000175938
SETD1A
ENSG00000099381
HSD3B7
ENSG00000099377
STX4
ENSG00000103496
VKORC1
ENSG00000167397
BCKDK
ENSG00000103507
KAT8
ENSG00000103510
PRSS8
ENSG00000052344
FUS
ENSG00000089280
dbSUPER
Number of super-enhancer constituents: 6
ID
Coordinate
Tissue/cell
SE_13828
chr16:30544521-30547982
CD34_Primary_RO01536
SE_24884
chr16:30543560-30547675
Colon_Crypt_3
SE_27951
chr16:30544223-30547967
Fetal_Intestine
SE_28916
chr16:30544073-30548009
Fetal_Intestine_Large
SE_31772
chr16:30543927-30547730
Gastric
SE_65737
chr16:30543926-30547882
Pancreatic_islets
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chr16
30545080
30545232
chr16
30545067
30545182
Enhancer Sequence
TGCTGAAAGA TAAGGAGGCG AGAGTTCAGG CTTGGCTCAT CCTGGTCATT GAATCCCACA 60
GCCCGCGTGG ACAGGGACAG GCCTGCTGGA CCCCCGACTG CTCCTAGGAG ATGGAGGAGT 120
GACACCTGTT CCTCGGCTGC AGAGCCAGAC AGAGCCTGGA GGGAGGGAAC AGTCCATTCC 180
GCCTCCGGGC TGGGGAAATG TCACCGCGGG GGAAGGGCAG AGATGACGTG AACATCTGGG 240
CCTGATCTGG AATAAGAAGC GGACACCTGG GGATATTCCA GGCAGAAGGA ACAGCACCAA 300
GAAAGGCAGA ACCAGGAGGG CATGGCCAAG TTCAGTGGGG CTGGATACTC TGCAAAAGCT 360
GAGGCAAGAA CTAAAGGAAG GAAATGGGAG GGCGGGATGT GGGGGCATAG GAACCATAGT 420
GCAGGAAAAC GACTGGAGCG GGTCATGATG TGGAGGTAGA GTCAACAGAA CCTAGAGGCC 480
GGGTGCAGTG GCTCATGCCT GTAATCCCAG TGCTTTGGGA GGCCGAGATA GAGGATCGCT 540
AGAGTTCGAG ACCAGCTCGG GCAACACACC AAGACCTCTA CCTCTTTAAA ATTTTTTTAA 600
TTAAAAAAAA AAAAAAAAAA CCAGCCAGGC GTGGTGGCGA GTGCCTTTAC AGTGTTAGGT 660
ACTCTGGAGG CCCACGCGGG AGGATTGGTT GAGCCGATTG CTTGAGCCCG GGAGTTCAAG 720
ACTGCAGTGA GCTATGATGG CGCCACTGCA CCTCAGCCTG GGCAACAGAG ACCCTGTCTC 780
TAAAACAAAA CAAAACAAAA AAGTCCCCGG AGTGTAGTGA CCACGCAGAG GTGAGGACTC 840
AGGGGCGGGT ATGGCAGGGC CAGAGCCCCC ATCACAGCCC CTTTCTAGGC TGCATCCCGG 900
AGCCAGGCAG GGGCTCAGCC TCCTGGCCGC AGTTGAGGAG GCAGTTCAGA GAGGAAACTG 960
CTAAGCAGGT AGCTGGAGGT GGCAGAGGGT ACCGGGATGG GACAGGAACA GAGAAGTCCC 1020
CATGGGACTG AGCACCCGAT 1040