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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS104-22382
Organism
Homo sapiens
Tissue/cell
HUVEC
Coordinate
chr16:1705300-1705870
Target genes
Number: 29
Name
Ensembl ID
UBE2I
ENSG00000103275
LA16c
ENSG00000261505
C16orf42
ENSG00000007520
GNPTG
ENSG00000090581
UNKL
ENSG00000059145
C16orf91
ENSG00000174109
CCDC154
ENSG00000197599
CLCN7
ENSG00000103249
TELO2
ENSG00000100726
TMEM204
ENSG00000131634
HN1L
ENSG00000206053
MAPK8IP3
ENSG00000138834
NME3
ENSG00000103024
MRPS34
ENSG00000074071
EME2
ENSG00000197774
SPSB3
ENSG00000162032
NUBP2
ENSG00000095906
FAHD1
ENSG00000180185
HAGH
ENSG00000063854
GFER
ENSG00000127554
SNORD60
ENSG00000206630
RP11
ENSG00000260260
TRAF7
ENSG00000131653
MLST8
ENSG00000167965
PGP
ENSG00000184207
ECI1
ENSG00000167969
AC009065.1
ENSG00000167970
RNPS1
ENSG00000205937
MIR940
ENSG00000216095
SNPs
Number: 1
ID
Chromosome
Position
Genome Version
rs79007183
chr16
1705794
hg19
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr16
1705411
1705465
Enhancer Sequence
TGTATCCTTT TCCAGCTAAA GCAAACCATC CAGGCTGCGC TGCCTCTGCT GCCCAGAGAT 60
GGACCACGCC TCCCTGTGCC TGTCATCGTC ATGGTCCCCG TGGGCAGAAC AGCCATGCTG 120
TGACATGGTG TACATCTGGA ACCATAACCT GGAGCCCCTT ATTCCCTGGG TGTGGAGCCC 180
CCTCTGTGGC CTTGCAGTGC TAGAACTCAG TCACAGCCAG CCCTCCACGA TGTCAGTGGC 240
CTGTGTCTGG CCCACGGGGT GTGGCCAAAG CATTCCTACC AGCAGGTTGA GCAAAACGAC 300
CAAGGGTCAG CCCAGCCTTC TTCACATCCA TGGCTGGCTC CCGGCCCTGC CTGCTCCCCA 360
CATAGGCGTG GTGCGTGTCA GGTGTGAATT TCCTGAAGGT ACTAAGTGCC CGGGTCAGCA 420
TTGTTGGGTA GTGGTGTGAG GAAAGCCACG GGTGGTGGCA TGATTTATAC CCTGGGGGAT 480
GCCAGTGGGG AGCGTGGCTC GTGTCTGTAC CCATGTGCCT GGTCAGCATC CCGACCTCAG 540
TGCTAGCCAG TGTGGGCCTT CCTTGACGGG 570