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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS101-16143
Organism
Homo sapiens
Tissue/cell
HT29
Coordinate
chr16:492120-493430
Target genes
Number: 47
Name
Ensembl ID
AL049542.1
ENSG00000256323
LA16c
ENSG00000261691
JMJD8
ENSG00000161999
MSLN
ENSG00000102854
FAM195A
ENSG00000172366
IL9RP3
ENSG00000226942
RPUSD1
ENSG00000007376
STUB1
ENSG00000103266
HAGHL
ENSG00000103253
NARFL
ENSG00000103245
C16orf13
ENSG00000130731
RHBDL1
ENSG00000103269
WFIKKN1
ENSG00000127578
RAB40C
ENSG00000197562
NHLRC4
ENSG00000257108
PIGQ
ENSG00000007541
ITFG3
ENSG00000167930
FAM173A
ENSG00000103254
METRN
ENSG00000103260
FBXL16
ENSG00000127585
Z98881.1
ENSG00000196674
GNG13
ENSG00000127588
LUC7L
ENSG00000007392
CHTF18
ENSG00000127586
CCDC78
ENSG00000162004
WDR90
ENSG00000161996
Z84812.3
ENSG00000233614
Z84812.4
ENSG00000260803
WDR24
ENSG00000127580
WASIR2
ENSG00000231439
NME4
ENSG00000103202
WASH4P
ENSG00000234769
TMEM8A
ENSG00000129925
AXIN1
ENSG00000103126
PDIA2
ENSG00000185615
ARHGDIG
ENSG00000242173
RGS11
ENSG00000076344
RAB11FIP3
ENSG00000090565
DECR2
ENSG00000242612
AL022341.3
ENSG00000228201
SNRNP25
ENSG00000161981
RHBDF1
ENSG00000007384
POLR3K
ENSG00000161980
MPG
ENSG00000103152
NPRL3
ENSG00000103148
RHOT2
ENSG00000140983
SOLH
ENSG00000103326
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr16
492392
492849
Enhancer Sequence
GCCACCGCGC CTGGCCTCAT GCTGTTTTTT TAAGAAACGG GGTCTCACTG TGTTGCCCAG 60
GCCGGAGCGC AGTGGCTGTT TATAGGCTCT GTCACAGTCA CTGCACCCTC CAGCTCCTGG 120
GCAGTCCTCC TGCCTCAGCT TCCTGCGTAG GTGGGACTCC TGGCCCATGC CACTGCACCC 180
AGCTTATGAT GCTGGTTTTT GAAATGGGGT TGCTATTCCC ATGGTGAGTG TCTTGGGGGA 240
GTTTGGGCAT GGTAGTTGGA GTTATAAATT CAACTGAGGT CTTTTGTTTC ATTCTGGAGC 300
GTTATTAGAA CCCTCGTGAA GGGGGTTGCT ATTTCAGGAG GAGCTGCAAT GGCCAACCAG 360
GAGTGTGCTG GTCTCCTTTC TGGTCTTCCT CCCGCTCAGC CGGGCTGCCG CTTCTGGTGT 420
CTGGTTGCTT CCATGGTTCT CTACTTCTGA AGTGGCAATC CAGGGTGGTC AGGCAGGGGT 480
GAATTGTCTT TCGGTGTCAT GCTACTTTTT TTCTGACGTA GTGGCAGTGT CTGCTGAGTC 540
GTCCCAAAGC ACAGAGATGT GATTTGCAGA AGGTATGTTG TGTCTTCGTG GGCAGGAGCT 600
GGAGCTCCAC CCTGTTGCTT TAGCAGGCGG CCTTTGACCA ATTAAGAGAG CAGGTCTTTC 660
TTGTTGGCGT AACTCTCCTG AGGGTCACAA CAGGCTCCGT GCTAGAGCGG TCATCTCTGC 720
AGATGTTTCT TCCTCTCTTC TACCACTCTC ACCCCTTATT TTTTTCCCGC TTGTTTACAA 780
AGTTTTATTT CATTCCAACA TCGGGTGGGT TGGTTTACTT TACTAAAATC CAAGAAAAAC 840
AAGGCTGACG TTTTTGCTGT TGGAAATGAA AAGCCCTTTT ATGAGAAAGT CCATCCCCGT 900
CAGCATGGCT TATTCTGTCT GGTGAGGAGA GAAGAAGCCA TGAAGACATT TCCTCTTGGT 960
GATTTAATTT TTAAGAACCC TCTTCAGGAA GCCAGCCCTG TGATGCATTT TAAGAGAAAT 1020
ACCAGTTAGT GAGGTTTCAT CAGCACTGAG GAACACTTGG CTCTCTCTTG CAGACTAAGA 1080
AATACCAAGC AGGAGGAGTC TTGGCATTTG GAACGGGTAA ATCAAGAACC TGCTCTTGTT 1140
GGCTTGCGAG TGCCTTTAAA GCGAAAGCAA GAAGCTTAGA AGGAAAACGT CACAGATCAT 1200
GCACGCTTAA AATAAAAACA TGCAAAAGAA GTAAATAAAA ATAATAACTT GCAAATAAAG 1260
GAGAAAATAA AAACCCCATC CAGCACCGTG AATCTTTTCA GCCTTCTGGC 1310