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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-21596
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr17:79992080-79993750
Target genes
Number: 60
Name
Ensembl ID
AZI1
ENSG00000141577
AC027601.1
ENSG00000260005
C17orf56
ENSG00000167302
LINC00482
ENSG00000185168
TMEM105
ENSG00000185332
RP11
ENSG00000262877
BAHCC1
ENSG00000171282
RP13
ENSG00000229848
ACTG1
ENSG00000184009
FSCN2
ENSG00000186765
C17orf70
ENSG00000185504
Y
ENSG00000207021
TSPAN10
ENSG00000182612
NPLOC4
ENSG00000182446
PDE6G
ENSG00000185527
CCDC137
ENSG00000185298
C17orf90
ENSG00000204237
HGS
ENSG00000185359
ARL16
ENSG00000214087
MRPL12
ENSG00000262814
SLC25A10
ENSG00000183048
GCGR
ENSG00000215644
AC174470.1
ENSG00000215621
FAM195B
ENSG00000225663
PPP1R27
ENSG00000182676
P4HB
ENSG00000185624
ARHGDIA
ENSG00000141522
ANAPC11
ENSG00000141552
ALYREF
ENSG00000183684
NPB
ENSG00000183979
PCYT2
ENSG00000185813
SIRT7
ENSG00000187531
MAFG
ENSG00000197063
PYCR1
ENSG00000183010
AC137723.5
ENSG00000235296
MYADML2
ENSG00000185105
NOTUM
ENSG00000185269
ASPSCR1
ENSG00000169696
STRA13
ENSG00000169689
LRRC45
ENSG00000169683
RAC3
ENSG00000169750
DCXR
ENSG00000169738
RFNG
ENSG00000169733
GPS1
ENSG00000169727
DUS1L
ENSG00000169718
FASN
ENSG00000169710
CCDC57
ENSG00000176155
SLC16A3
ENSG00000141526
AC132872.1
ENSG00000184551
CSNK1D
ENSG00000141551
CD7
ENSG00000173762
SECTM1
ENSG00000141574
TEX19
ENSG00000182459
UTS2R
ENSG00000181408
HEXDC
ENSG00000169660
C17orf101
ENSG00000181396
C17orf62
ENSG00000178927
NARF
ENSG00000141562
FOXK2
ENSG00000141568
WDR45L
ENSG00000141580
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chr17
79993261
79993526
chr17
79992322
79993258
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH17I082034
chr17
79992681
79992930
Enhancer Sequence
CCTCTTGCCT CTCACTACCT GCCCTTCTGT CCTGGGGCGG TTTGCTCCTA ATTCCCCTCT 60
GTGATGGTGC AGAGCGGGTC CATCACACCC CAGCCGACCC CAGCCGCACT TCAGAGCTGA 120
GTTCCCAAAG GCAGCACTAA GCTTCCTCCA CCCTACCCCA GGGGAAGAGG GGGCCTGCTG 180
AGCTGCTCAG CCCCCCAAAG GAGCCGACCC AGATCAAAGC AATAGCTAGT GCATTGAGCC 240
CTAGGGATGA TTACTTGGCT GTGTACAAGG CCTCCCTCAG GCTGATTTGT GCCTCTGGGA 300
GGGCACATGT CAGGGAGGGG TGGGGAGAGG CGGGCCAGTT CTCAGGCAGC GCCTGTTGTG 360
CTGACCGGGA AGGTCTGAAA AGAGGCTGAA GCAGGTCAGG CCTCTCTGAG CCTCGTGGGA 420
GCCGAGGCAG GCTCCCCGCA TCCCTCAACT CCTCTGGCTG GCACCGGGAG TAAGGGCAAT 480
CCAGGCAGAG GGGCAGGGTG GAGGAGGGCG CGGGGGTCGG GGTGTGGTGT GGAGAGTGAA 540
GAGAGCAGTG ACCCAGCACA GTCCGCTGAC GCTGAAGCCA GAATCAGTGG GCCCGGAGCC 600
ATGGTCCCGG GATTGGAGTC ACTCGGGATT GGAGGGTGCC ATGAGGTCCC GGGATTGGAG 660
TCACTCGGGA TTGGAGGGTG CCATGAGGTC CCGGGATTGG AGTCACTCGG GATTGGAAGG 720
TGCCATGAGG TTCCAGGATT GGAGTCACTC GGGGTTGGAG GGAGCCATGG TCCCGGGATT 780
AGAGTCACTC GGGATTGGGG GGTGCCATGA GGGCCACTGT CTGCTTCCGC CTTGTGCTGT 840
GTGGGGGCAG CTCCTACTGG CTCAGGAAAG CCAACTGCTG AATTCTCAAC AATTTTGCTA 900
GCCAGTTGTT AATGATCATT AACAAATTAT AGAAGCTTAC AATTTGTGTT ATTAAAAGCA 960
AAATCGGCAA ACGTCACTTC CTACTTATTT CTGCATACAC GACTGTTTTC TCTGCCCCTC 1020
GGTTATGTAC ATCTGTGGGA CCTATGGACA CAAACACCAC ATAACAGGGT GCTGAGGGCA 1080
TCTCCTCCAG CTCCACGTTA AATGACATCT AACTGGTAGC TTGAAATCAG CCGTGGTGGG 1140
AGGAGGCTTG ACTTATGGTT ACTTGTCTAG ACTTCAGATG ATAAAATGCA GATTAGACTT 1200
CAGGGTGCTG TGTCTATGCT CATTACATTG TGAATAGCAC AAGTTGAGGA AACGCTCTTC 1260
TAGTTTCCGA AAACCATCAT CTGATTCAAC AAAGTGGCTC AGATCACCGA CGAAGTGGAG 1320
AAGCTTGACG TTCTCCTTGT TTCCCTTTTG TCTTACTCAT TAGCTTGAAG GAAGAGGAGC 1380
CAACTGTACA CTCACAGAGG GGGCCATCAA CACTCACATG CACACACCGT CTCACCCCAG 1440
AGGTTCTGGA CAGGCCCGAA GGCCAACCTT GCTGAAATTC ACCACCCTCT TTGGGAGGTG 1500
ACCTTTCACC ACCTCCCACC TCCCTGACAG AGAACTGGCC AGGCCTGAAA ACCTCAGGAG 1560
TGGGAGCCAC GCTCCCCCTT GGATTGGAAT GTGAATGTCA TGGGTCTCTG CCCGCGTTCC 1620
ACACCTGGCC CCAAGCCCCC AGCTACCTGC TGGCAGCCTA GGAATAGCAC 1670