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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS092-16565
Organism
Homo sapiens
Tissue/cell
HFF
Coordinate
chr14:75529360-75530170
Target genes
Number: 28
Name
Ensembl ID
ALDH6A1
ENSG00000119711
LIN52
ENSG00000205659
AC005519.4
ENSG00000258559
ABCD4
ENSG00000119688
RPS2P2
ENSG00000177776
RP3
ENSG00000259005
RAP1AP
ENSG00000258769
ISCA2
ENSG00000165898
NPC2
ENSG00000119655
CTD
ENSG00000258425
LTBP2
ENSG00000119681
RP11
ENSG00000258439
KIAA0317
ENSG00000119682
FCF1
ENSG00000119616
YLPM1
ENSG00000119596
PROX2
ENSG00000119608
DLST
ENSG00000119689
RPS6KL1
ENSG00000198208
PGF
ENSG00000119630
EIF2B2
ENSG00000119718
MLH3
ENSG00000119684
ZC2HC1C
ENSG00000119703
ACYP1
ENSG00000119640
NEK9
ENSG00000119638
TMED10
ENSG00000170348
FOS
ENSG00000170345
JDP2
ENSG00000140044
C14orf1
ENSG00000133935
SNPs
Number: 1
ID
Chromosome
Position
Genome Version
rs572568967
chr14
75529360
hg19
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr14
75529420
75529637
Enhancer Sequence
ACAAAAAAAA AAAAAAAAAA AAAAGAAGTT TTGCAGTCCT AACTCATTAT CTGTGGGATT 60
AGCGACACAC TGGGAAGGCA ATAGCCAATA CCTACAGAAG GCAGAGGGTA AATTGAGCTT 120
GCATTTGTGT GTGCCTGTTG AGGGAAGATT AGCCACATTA AAGCAGAGGT AGAGGCTGCC 180
AACAGTTTGT CCATCCCCTC AAATAATCCT TTATTGCTCT AGGAAGAATA CCAGGCTCCA 240
CATTCAGTGT TCCCATCACC TATTCTGGAA TGGATAAAGA GTTTTTAATA AGAAAAACGT 300
CAGCTGGAAA AGGTAAATGT TCTTTCAAAA CCAAAAAAGA ATAGAAAGAA ATTAAGTGGA 360
GAACTGAGGG AAGCTTGGAG AAAGAGGTCT GAAGAAAGTG CAGCAGCTGC AGAGGAAGCA 420
TTTATATATG TTATATACAT GACATCAGGT CATCTAAATG CCAGCTCTTC AATCAATGTT 480
AGCCTTTCTA TAAGAAACCT GACTTGGTTT GATGATGCCA CAACGGCGAG CACTGGGGAA 540
GCCCTCTATT TCCCTTGGAA GAGAGAAGCT CATTAATATG TGTATCTAGA TGCTCAGGCA 600
CCACTGACTA ATAATAACAG CAGGGTGATC TTCCATTTAC ACCATGTTTT ACCGATTGCA 660
CAGCATTTTC ATACTCATTG CTCTACAAAC TACCTCTTTG CCATGCAGCT ACCAAATAGC 720
CAGCGGCTTC TAGTTCACAT TTGTCAAGAA CACGTCCCTT GTTCCTATGC CCACAACCTA 780
GGTTACCACC CCAAAGCCTG CAGGCCACAT 810