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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS073-14848
Organism
Homo sapiens
Tissue/cell
GM19238
Coordinate
chr9:139759500-139760630
Target genes
Number: 28
Name
Ensembl ID
FAM69B
ENSG00000165716
SNHG7
ENSG00000233016
LCN10
ENSG00000187922
LCN15
ENSG00000177984
TMEM141
ENSG00000244187
KIAA1984
ENSG00000213213
C9orf86
ENSG00000196642
RP11
ENSG00000228544
NCLP1
ENSG00000213212
C9orf172
ENSG00000232434
PHPT1
ENSG00000054148
MAMDC4
ENSG00000177943
EDF1
ENSG00000107223
TRAF2
ENSG00000127191
FBXW5
ENSG00000159069
C8G
ENSG00000176919
LCN12
ENSG00000184925
C9orf142
ENSG00000148362
CLIC3
ENSG00000169583
DPP7
ENSG00000176978
SSNA1
ENSG00000176101
TPRN
ENSG00000176058
NDOR1
ENSG00000188566
C9orf169
ENSG00000197191
TUBB4B
ENSG00000188229
FAM166A
ENSG00000188163
COBRA1
ENSG00000188986
C9orf167
ENSG00000198113
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
GGAGAGTGAA TTTGGTTTTG ACTGTGCAAC CAGTAAGGGT AGGGCAGACC AATGAATCCC 60
TGTCACCAGA GCCCCAGCGC ATCCTGGCCC AACTGGCCTC AAAGGCTTCA GCCCTAGGCC 120
ACCTGAGGGT ACGAATGAGG CAGAGGCGGT GACTAAACTG TCCTCCCTAT TACATCAGAC 180
TCACAACTGA CCCTCGGATC CATCAGCCAC ATTGGTAATC TCCTTCCACA AGTACTGTTC 240
AGGGCACGCC CATCTTCCAC CTGTGCAACA GGGTCCACCT GCTCATGGGG TCCCCTGAAG 300
CAGGCACTCT CTACAGCCTG TGATGCACCC AGGCAGGCTC CCTGGGCAGT ATCTGACCAG 360
CGGAGACCAG TAGAACCAAG CAGGTCCCAG GCAGAGAGAA AACTCTCAGG GAGGAGCCTA 420
CCCCCTGTCC CCAGCTCCCA CTCAGGTCAC TAACCTCTGC CCCGTCACCC AGTCTCCCGC 480
CCCAGGCCCT CAACTGCTGT CCAATGGCCC CCAGCCCTAT CCCAACCCCA ATTCCCCACC 540
TTCATCGCTG GTTCCTGCTG CTTGCCCCAG TCCCCACCCC TGTCCTAAGC CCTGTACCCC 600
ACTCTACCCT GTTCTTCCAA GCCCTGTCCC CATCTCCATC CCTGCCCCCG TTCCCAGTGC 660
CCACCCTGGT TCTCTGTCCC CTATCCTCAC ACAAGGCCCC CAGCCTTGTC CCCGTCCCCG 720
TCCCCACCTC CTGCCTCTGT CCTCACACCT GTCCCCACCA ACAGTCCCTG CCCCTATCCC 780
CTCCCCGCCC CACCCTGGCA CTGGTCCCGG CCCTATCGCC TGCCCCTTGC CCCGTCCGGT 840
TCCCTGCTCC TCTCCTCCTC CAGTCGCCCG CCCCCTGCCT CCTGGGTCCG TCCATCCCCT 900
CCTGGGTCCG CCCCCCACCT TCCCACCCCT GTCCTGGCCC GGTCCTCCTA CCCCTGCGAT 960
TCGCCCCGCC CTTCGAACCC CGTCCTGCCC CCGGCACCCC AGCCTTGTCC CCGTCCCCTG 1020
CGCCCTGTCC CAGGCCCCGC CTGCCCTTCC CCGAGCCCCC TGCCCCACGG TCCGTGGCCC 1080
CGGCCCAGCG TCCGCCCCGC CCGGCCCGGC CGCTCCTCAG TCAGCAAAGC 1130