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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS088-26360
Organism
Homo sapiens
Tissue/cell
HeLa-S3
Coordinate
chr19:3526380-3526970
Target genes
Number: 31
Name
Ensembl ID
GNA11
ENSG00000088256
NCLN
ENSG00000125912
NFIC
ENSG00000141905
C19orf77
ENSG00000095932
DOHH
ENSG00000129932
FZR1
ENSG00000105325
C19orf71
ENSG00000183397
MFSD12
ENSG00000161091
HMG20B
ENSG00000064961
GIPC3
ENSG00000179855
TBXA2R
ENSG00000006638
C19orf29
ENSG00000105298
PIP5K1C
ENSG00000186111
TJP3
ENSG00000105289
APBA3
ENSG00000011132
MRPL54
ENSG00000183617
RAX2
ENSG00000173976
MATK
ENSG00000007264
ZFR2
ENSG00000105278
ATCAY
ENSG00000167654
ITGB1BP3
ENSG00000077009
MIR637
ENSG00000207733
DAPK3
ENSG00000167657
EEF2
ENSG00000167658
PIAS4
ENSG00000105229
AC016586.1
ENSG00000205147
ZBTB7A
ENSG00000178951
MAP2K2
ENSG00000126934
CCDC94
ENSG00000105248
SH3GL1
ENSG00000141985
CHAF1A
ENSG00000167670
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chr19
3526387
3526481
chr19
3526675
3526786
Enhancer Sequence
CACGGTAAGC CTGCGGCACC CCCCACCCGG GAGCTGGCTC CCAGTGCAGC CTCCCCGGCC 60
CCCCACCTCC CAGGCACCAG CTCTGCCTCC CCGAGCCCGG TTCTCGGGCC CAGCCACGGC 120
TCAGCACCCC CGCCCTGACC CTGTTCCTTA GCCAGGTCAG GGGCCCTGGG ATCTGAGGCT 180
GGAGGTCTAG CAGGTAAACT GGGATGTGGG GGTGCGGGAG GAATCCAGGC TCAGCCTGTT 240
GGGCTTTTTC TCCCCACACC AATGCTACCT GGGGTCCCGA ACACCCAAGC CGGTGGGGGT 300
CCTGCCCGTA GGGGGCAGTA CTGGGTCCTC CCACAGGGCC CCACTCTGTC CACATGATCC 360
GGGAGCTCAA AGGCAGGATC ACACGGAGCC TGGCTTGGGT CCCTCGAGAG AGGGCGGGAG 420
GGGTGGGGGG TCCGCAGTCC CCGCCAGGAA GGCGCCTGCC TTTTTACAGC TGCTCCACAC 480
AGGGTCTCAG CACCTGCCTT AGGGCTATGA GCTGTACCGG GAGCGTGGGC TGCTGGGGGG 540
CTCTGAGGGT CCTGCGGCCT GGGCGTGCGC TCAGCTGGCA TGTCCCCCGC 590