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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS098-59169
Organism
Homo sapiens
Tissue/cell
HSMM
Coordinate
chr9:139760090-139760630
Target genes
Number: 31
Name
Ensembl ID
EGFL7
ENSG00000172889
AGPAT2
ENSG00000169692
FAM69B
ENSG00000165716
SNORA43
ENSG00000199437
SNORA17
ENSG00000212487
SNHG7
ENSG00000233016
ATP6V1G1P3
ENSG00000224662
TMEM141
ENSG00000244187
KIAA1984
ENSG00000213213
C9orf86
ENSG00000196642
RP11
ENSG00000228544
NCLP1
ENSG00000213212
C9orf172
ENSG00000232434
PHPT1
ENSG00000054148
MAMDC4
ENSG00000177943
EDF1
ENSG00000107223
TRAF2
ENSG00000127191
FBXW5
ENSG00000159069
C8G
ENSG00000176919
C9orf141
ENSG00000198454
PTGDS
ENSG00000107317
LCNL1
ENSG00000214402
C9orf142
ENSG00000148362
CLIC3
ENSG00000169583
C9orf139
ENSG00000180539
ABCA2
ENSG00000107331
NPDC1
ENSG00000107281
SAPCD2
ENSG00000186193
UAP1L1
ENSG00000197355
MAN1B1
ENSG00000177239
COBRA1
ENSG00000188986
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
CCTGTACCCC ACTCTACCCT GTTCTTCCAA GCCCTGTCCC CATCTCCATC CCTGCCCCCG 60
TTCCCAGTGC CCACCCTGGT TCTCTGTCCC CTATCCTCAC ACAAGGCCCC CAGCCTTGTC 120
CCCGTCCCCG TCCCCACCTC CTGCCTCTGT CCTCACACCT GTCCCCACCA ACAGTCCCTG 180
CCCCTATCCC CTCCCCGCCC CACCCTGGCA CTGGTCCCGG CCCTATCGCC TGCCCCTTGC 240
CCCGTCCGGT TCCCTGCTCC TCTCCTCCTC CAGTCGCCCG CCCCCTGCCT CCTGGGTCCG 300
TCCATCCCCT CCTGGGTCCG CCCCCCACCT TCCCACCCCT GTCCTGGCCC GGTCCTCCTA 360
CCCCTGCGAT TCGCCCCGCC CTTCGAACCC CGTCCTGCCC CCGGCACCCC AGCCTTGTCC 420
CCGTCCCCTG CGCCCTGTCC CAGGCCCCGC CTGCCCTTCC CCGAGCCCCC TGCCCCACGG 480
TCCGTGGCCC CGGCCCAGCG TCCGCCCCGC CCGGCCCGGC CGCTCCTCAG TCAGCAAAGC 540