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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-24736
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr19:55738930-55739550
Target genes
Number: 28
Name
Ensembl ID
U6
ENSG00000199308
CTC
ENSG00000243494
RDH13
ENSG00000160439
EPS8L1
ENSG00000131037
PPP1R12C
ENSG00000125503
TNNT1
ENSG00000105048
TNNI3
ENSG00000129991
DNAAF3
ENSG00000167646
SYT5
ENSG00000129990
PTPRH
ENSG00000080031
TMEM86B
ENSG00000180089
PPP6R1
ENSG00000105063
HSPBP1
ENSG00000133265
BRSK1
ENSG00000160469
COX6B2
ENSG00000160471
IL11
ENSG00000095752
TMEM190
ENSG00000160472
RPL28
ENSG00000108107
UBE2S
ENSG00000108106
ISOC2
ENSG00000063241
ZNF628
ENSG00000197483
NAT14
ENSG00000090971
ZNF784
ENSG00000179922
ZNF580
ENSG00000213015
ZNF581
ENSG00000171425
CCDC106
ENSG00000173581
U2AF2
ENSG00000063244
EPN1
ENSG00000063245
dbSUPER
Number of super-enhancer constituents: 1
ID
Coordinate
Tissue/cell
SE_65612
chr19:55737613-55741863
Pancreatic_islets
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr19
55739031
55739110
Enhancer Sequence
CCTGGCGGGA GAGGGGTGGG GTACCAGTGA GGAAGGCCCA TCCTGGGAAT GGCCCCGAGG 60
TCACCCCTCA GGGCCTAAGA GAAGGACCAT CCCAGAGCAC CAGGCCCCAC CCTGGCCGAG 120
CCTCCTTGCA GGTCTCCCCA CATGCAGTGT CCATCCTTGC TCTGCTCAGA ACTGCCAGGA 180
GGCCCCACCT TCCCTTGGCC TCCAAAGCCC CATGGCCTCC AGCTCTCCAG CCACTCTGCG 240
CCAGCCACCC TGGCCTGCTG GGCTACAAGC ACCTGACACG TCCCTGCCCC GGAGCCTTTA 300
CACTCGCCCT TCCTCCACAC AGGCATACAG CCCTTCAGCT CTGCCCAAAT GTGACTTCCT 360
CAGTGAGGCC TTCCTCAGCA ACCCTGCTTC AAACTGCAGT ACCTCCAGCA GGTCCTCACT 420
GCCCTCTGCG CCACCTCAGC TACTGCCCTA ACACCGCCTG CCCCCACCCC TCGCTGGAGC 480
GTGAGCTGCC TCGGTCACGG CTGCGCCCCC CACTGTGCCT TTGACCACTG GAGCTCTCAC 540
AGGAGCCCTC TGCACCCAGG CTCCCATCCA AGTGCTGGGG CCTCTCTCAC ACGGGCATCT 600
GGAAAGCGTC ACAGCACCTT 620