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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS086-07471
Organism
Homo sapiens
Tissue/cell
HEK293
Coordinate
chr19:49513320-49513740
Target genes
Number: 37
Name
Ensembl ID
KDELR1
ENSG00000105438
GRWD1
ENSG00000105447
CYTH2
ENSG00000105443
SPHK2
ENSG00000063176
RPL18
ENSG00000063177
DBP
ENSG00000105516
FUT1
ENSG00000174951
FGF21
ENSG00000105550
BCAT2
ENSG00000105552
HSD17B14
ENSG00000087076
PLEKHA4
ENSG00000105559
PPP1R15A
ENSG00000087074
TULP2
ENSG00000104804
NUCB1
ENSG00000104805
CTD
ENSG00000260366
DHDH
ENSG00000104808
BAX
ENSG00000087088
FTL
ENSG00000087086
GYS1
ENSG00000104812
RUVBL2
ENSG00000183207
LHB
ENSG00000104826
CGB
ENSG00000104827
CGB5
ENSG00000189052
CGB7
ENSG00000196337
NTF4
ENSG00000167744
AC008687.1
ENSG00000225950
SNRNP70
ENSG00000104852
LIN7B
ENSG00000104863
C19orf73
ENSG00000221916
PPFIA3
ENSG00000177380
HRC
ENSG00000130528
TRPM4
ENSG00000130529
AC011450.2
ENSG00000235555
TEAD2
ENSG00000074219
PTH2
ENSG00000142538
FCGRT
ENSG00000104870
SCAF1
ENSG00000126461
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr19
49513528
49513692
Enhancer Sequence
CAGGTGCGGC CGGGACTCCC GGGATCCCCT CGCCCCCAGC ACTGGGGTGT TTTCATCTCC 60
TCCATCACCC CCTTGACCCA TGGGGTCTGG ATCTTCCTGT TACCCTGACT GTTTGTCCTG 120
GTACTCCTGG GTCTTCCCTG TAACCCTAGG ACAGCAGGGC CCCTCAGCCT GGCACTATAG 180
CTTCGCATGG CCACATGTGG CCTGTGGCTT CTAAGGTCCT CCGGGAGCCC CCGTGACCCT 240
CAGCGCTCTG GAATGTCCCT AGTCCTGACT ACCTCCTGGG CCTGGGGTTT CCAGATGACC 300
CCATTTAGCC TCCCAGCTCC ATTTCCTGGA GCTCCAGTCT CCCCCAGACA GAGGGCTTTA 360
GGGGCCCCCT TCATGCCCTT CCCTGCCCTG TCTCCGCCGT TCTTCCCCCA CCCCCGCCCC 420