HOME
BROWSE
DOWNLOAD
LINKS
HELP
EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS092-23238
Organism
Homo sapiens
Tissue/cell
HFF
Coordinate
chr19:55916900-55918180
Target genes
Number: 29
Name
Ensembl ID
RDH13
ENSG00000160439
PPP1R12C
ENSG00000125503
TNNT1
ENSG00000105048
TNNI3
ENSG00000129991
SYT5
ENSG00000129990
PTPRH
ENSG00000080031
TMEM86B
ENSG00000180089
PPP6R1
ENSG00000105063
HSPBP1
ENSG00000133265
BRSK1
ENSG00000160469
SUV420H2
ENSG00000133247
COX6B2
ENSG00000160471
IL11
ENSG00000095752
RPL28
ENSG00000108107
UBE2S
ENSG00000108106
ISOC2
ENSG00000063241
ZNF628
ENSG00000197483
NAT14
ENSG00000090971
SSC5D
ENSG00000179954
AC008735.15
ENSG00000231274
ZNF579
ENSG00000218891
FIZ1
ENSG00000179943
ZNF524
ENSG00000171443
ZNF865
ENSG00000261221
ZNF784
ENSG00000179922
ZNF580
ENSG00000213015
CCDC106
ENSG00000173581
U2AF2
ENSG00000063244
EPN1
ENSG00000063245
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr19
55917170
55917359
Enhancer Sequence
AATGGCTGGG TTCCTAGGGG GCCACAGGAC CTCCCCCAAA ACCTCAGAGA TGATGCCCAT 60
CTTGCAGCCC CCACCTGTGT CACTATCAAG CTCGTCTGCA CCCTCCTGGA TCCCCCGTCT 120
CAGCCCAACT GACCACTCCA GTCACAGGCC CTTCCCAGGT GGCAGGGACC CAAGTACGCA 180
CTTTCCTATA AGATGCCCAT TTATATGCCT TTCAGATCAA GGATCCAACT GTCTGTTAAT 240
TCCACAGCCT CCCAACCCAG TGAACGCCTC TCCCACTCAC CCACTTGCTT GGGTCAAAAT 300
ACTGTCCCTC CCCTAGCCCA TCAGCAGCCT GAGCACCGGC CTGCTAGGTC CTCCCCTGAA 360
TCTCATCCCA TCTCCAAGGC TAGCTTCCTG GCTGGCCTCT GGGTTCTTCC CCCTGCCAGG 420
CCGGCTCTCC TCACTACAGT CAATAGGAAC TTTGGAGGGA TTTGTCACAC CCCTGCTTTA 480
AACCTTCCAC CAGCTTCCTC TACAAACTCC TTGAAGAGGC CTAGAAGCCC TAAAAGAGCT 540
TGGCAGCTTC ATCATCAACT TTCTTCATGT GTTTTTACCA AGCGCCCAGC TCCACCTGCC 600
CAAGGGCCTT TCTGGAGCCT TCCTATTGTC ATGATCCCGC GCCCTCTGCA GCAAGGCATG 660
AAGGACCTCA ACTGTCACCG CTGCCAGGTC TTTCCTGACC ACCTACCACC ATCACCACCG 720
TGGACTAGAC CATTCCTTCA CAGGCTCTGC TCAAATCCTG ACTTTGTAGG AATTCTGGTG 780
ATAACAGAAA TGTAGCCTGC ATGAAACAGT ATTCTAAATC ACTCCGCAAA TCATGTGACC 840
CGCAAATCAT TCATGACCCG TCTCCCCACG ATCTGCATCT GGCTTGTTTC CTCATCCCTG 900
ACACTCACAG CAGGATGGAG TTTGAGATCA CCTGGCCCAC CCTCCCAGGC CCTTGCTGAC 960
ACCATTCCCA CCACCTGGAG CTCTCTTCCC ATTCCTACTT AATTCCTACC CACCCTCAGG 1020
TCCAGGGAAG CCATGTCTGA AAGCCTTGCT TCAAATCTAG AGTACCGTCC CATGATATAC 1080
TAACTCAATG ACCAGATATT TCTCAACCCT TGTGGGAAAA GAGTACATAA TTGTCATTTG 1140
TGGCGTCCTG CCCTGTCCAC CAATGCATCC CAACACCTGA CACGAGGCCA GCCTGTAATG 1200
GGTACTTCCC GCTAGGGTGA TCTAGAGCAG GGTGATGGAG GATCTAAGCA GCAGCCCCTT 1260
CTCTTTTTCC TTCCAAACTC 1280