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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS105-84017
Organism
Homo sapiens
Tissue/cell
IMR90
Coordinate
chr9:139759430-139760630
Target genes
Number: 27
Name
Ensembl ID
EGFL7
ENSG00000172889
AGPAT2
ENSG00000169692
FAM69B
ENSG00000165716
SNORA17
ENSG00000212487
SNHG7
ENSG00000233016
TMEM141
ENSG00000244187
KIAA1984
ENSG00000213213
C9orf86
ENSG00000196642
RP11
ENSG00000228544
NCLP1
ENSG00000213212
C9orf172
ENSG00000232434
PHPT1
ENSG00000054148
MAMDC4
ENSG00000177943
EDF1
ENSG00000107223
TRAF2
ENSG00000127191
FBXW5
ENSG00000159069
LCN12
ENSG00000184925
PTGDS
ENSG00000107317
LCNL1
ENSG00000214402
CLIC3
ENSG00000169583
ABCA2
ENSG00000107331
NPDC1
ENSG00000107281
ENTPD2
ENSG00000054179
SAPCD2
ENSG00000186193
UAP1L1
ENSG00000197355
MAN1B1
ENSG00000177239
TMEM203
ENSG00000187713
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr9
139760251
139760347
Enhancer Sequence
CACAGATGCT GCCACGCAAT TATTCCCATG ACTCCTAGCT TGTGGCCATT AAGTTTCCTT 60
TAAAAGAAAA GGAGAGTGAA TTTGGTTTTG ACTGTGCAAC CAGTAAGGGT AGGGCAGACC 120
AATGAATCCC TGTCACCAGA GCCCCAGCGC ATCCTGGCCC AACTGGCCTC AAAGGCTTCA 180
GCCCTAGGCC ACCTGAGGGT ACGAATGAGG CAGAGGCGGT GACTAAACTG TCCTCCCTAT 240
TACATCAGAC TCACAACTGA CCCTCGGATC CATCAGCCAC ATTGGTAATC TCCTTCCACA 300
AGTACTGTTC AGGGCACGCC CATCTTCCAC CTGTGCAACA GGGTCCACCT GCTCATGGGG 360
TCCCCTGAAG CAGGCACTCT CTACAGCCTG TGATGCACCC AGGCAGGCTC CCTGGGCAGT 420
ATCTGACCAG CGGAGACCAG TAGAACCAAG CAGGTCCCAG GCAGAGAGAA AACTCTCAGG 480
GAGGAGCCTA CCCCCTGTCC CCAGCTCCCA CTCAGGTCAC TAACCTCTGC CCCGTCACCC 540
AGTCTCCCGC CCCAGGCCCT CAACTGCTGT CCAATGGCCC CCAGCCCTAT CCCAACCCCA 600
ATTCCCCACC TTCATCGCTG GTTCCTGCTG CTTGCCCCAG TCCCCACCCC TGTCCTAAGC 660
CCTGTACCCC ACTCTACCCT GTTCTTCCAA GCCCTGTCCC CATCTCCATC CCTGCCCCCG 720
TTCCCAGTGC CCACCCTGGT TCTCTGTCCC CTATCCTCAC ACAAGGCCCC CAGCCTTGTC 780
CCCGTCCCCG TCCCCACCTC CTGCCTCTGT CCTCACACCT GTCCCCACCA ACAGTCCCTG 840
CCCCTATCCC CTCCCCGCCC CACCCTGGCA CTGGTCCCGG CCCTATCGCC TGCCCCTTGC 900
CCCGTCCGGT TCCCTGCTCC TCTCCTCCTC CAGTCGCCCG CCCCCTGCCT CCTGGGTCCG 960
TCCATCCCCT CCTGGGTCCG CCCCCCACCT TCCCACCCCT GTCCTGGCCC GGTCCTCCTA 1020
CCCCTGCGAT TCGCCCCGCC CTTCGAACCC CGTCCTGCCC CCGGCACCCC AGCCTTGTCC 1080
CCGTCCCCTG CGCCCTGTCC CAGGCCCCGC CTGCCCTTCC CCGAGCCCCC TGCCCCACGG 1140
TCCGTGGCCC CGGCCCAGCG TCCGCCCCGC CCGGCCCGGC CGCTCCTCAG TCAGCAAAGC 1200