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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS133-10820
Organism
Homo sapiens
Tissue/cell
melanoma
Coordinate
chr16:1372860-1374730
Target genes
Number: 38
Name
Ensembl ID
JMJD8
ENSG00000161999
RPUSD1
ENSG00000007376
STUB1
ENSG00000103266
FAM173A
ENSG00000103254
LA16c
ENSG00000260964
METRN
ENSG00000103260
WDR90
ENSG00000161996
WDR24
ENSG00000127580
RHOT2
ENSG00000140983
LMF1
ENSG00000103227
UBE2I
ENSG00000103275
BAIAP3
ENSG00000007516
C16orf42
ENSG00000007520
GNPTG
ENSG00000090581
UNKL
ENSG00000059145
C16orf91
ENSG00000174109
CCDC154
ENSG00000197599
CLCN7
ENSG00000103249
TELO2
ENSG00000100726
TMEM204
ENSG00000131634
IFT140
ENSG00000187535
CRAMP1L
ENSG00000007545
HN1L
ENSG00000206053
MAPK8IP3
ENSG00000138834
NME3
ENSG00000103024
MRPS34
ENSG00000074071
EME2
ENSG00000197774
SPSB3
ENSG00000162032
NUBP2
ENSG00000095906
FAHD1
ENSG00000180185
MSRB1
ENSG00000198736
NDUFB10
ENSG00000140990
RPS2
ENSG00000140988
SNHG9
ENSG00000255198
TBL3
ENSG00000183751
GFER
ENSG00000127554
AC005606.14
ENSG00000261790
E4F1
ENSG00000167967
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4
Chromosome
Start
End
chr16
1373890
1373944
chr16
1374426
1374530
chr16
1373330
1373759
chr16
1374540
1374692
Enhancer Sequence
GATGATGGTG CATGCCTGTA GTCCCAGCTA TTTGGGAGGC TGAGGTGGGA GGACTGCTTG 60
AGCCCAGGTG GTTGATGCTG CAGTGAGCCA AGATTGCAGC CTGGGTGACA AAGTGAGACC 120
CTGTCTCAAA AAAAAAAAAA AAAGCATGCC GGGCGCGGTG GCTCACGCCT GTAATCCCAG 180
CACTTTGGGA GGCCAAGGTG GGCAGATCAC GAGGTCAGGA GATTGAGACC ATCCTGGCTA 240
ACACGGTGAA ACCCCATCTC TAGTAAAAAT AAAAAAAATT AGCCGGGCGT GGTGGCGCAC 300
ACCTGTAACC CCAGCTACTC GGGAGGCTGA GGCAGGAGAA TGGCTTGAAC CTGGGAGGCG 360
GAGCTTACAG TGAGCCGAGA TCACGCCACT GCACTCCAGC CTGGGCAACA GAGCCAGACT 420
CTGTCTCAAA AAAACAAAAC AAAAGGCAAA TGTTTTCCTG CCTAGCCCTT AGATGGTCTG 480
CCATCCCCAG CATGGTGTGG GCGTGAGCTC TGTCTGGCCT GCACCCCATT TGCCGACCAT 540
CTCCAGAGCT GGGCTGTGGC TCCCATCTGC GGCGTGGGCT GGGCAGGGTT GCAGTCCCCC 600
GCCCCGTGTG ACTCTCCCCA GCGTCTCCTG GGCTTGGTGC CTGCTGGGCT GCACTGTACA 660
CTTGCGTGCA CGTAAACAAA CGTTCTTTCT CCTACACACA TCCGCTTGAA AAGCACCCTT 720
TGTGAAGCAT GTGTGCGGGT TTCAGATCGT TTTTCCTGGG TTTCCTGGAG GCCTTGGACC 780
GTGTTCCTGC CCTGGCAGGT GCCTTTTCTC GGGGCCTCTG CTTGGTCAAG GAAGAGCTGG 840
GACGTGTAGC CACCGCCTCT GGTTCCTTCC ACGCCCACCC AGCTGAGCTG CTCTGCCCTG 900
GGGCCGGCTG GTGGCCCAAG GAGGGCGCTG GGGTCTGGGC TGCGGTCCAG GCCCTTGGCG 960
TGGGTGGGGG TGGCACCGGC GCTGCTGCCG TCCTGGGCTG TTCCACCATG CAGAGTGAGG 1020
CTCAGTGTCT CAGACCAGGT CCAATCCTGG CGAGACTGGC AGGACTGCGA CCCCAGGAGC 1080
CACCTCCATA AATGTCATGG TGTTCCCCCA TCCTCAGGGT CACACTGCAC CCTGTGACCC 1140
ATCAGCCCCT AGGTGCAGCC TCGGCCGCCC TCCCGCCCAC CTGTTTTGCC CGGGCAGTGT 1200
GTGCCATGCC ACTCTCCTGG GCAGCTGCTT GCAGGCTGAG CCTCACTCTA CCCAGCTCCA 1260
GACCTGTTCG CTGATGCCCC TGCACTGCCC AGCTCGGGCA CAACGCCTTC TCAACCAGGC 1320
CTGCCTTCCC ACACCTTTGC CCCTGCGGCT GAGAGCCTCA TGGAAAAACC CTCCAGAAAT 1380
TGGTGTCTAT TTTTGGGAAT TAACAAAAAC AGTGGCAAGC AGTCAGTGTT TTCAGTTTAT 1440
TAGGACTGTC CCCAGACCTA CAGAAAAGAG AAGCTGCTGA TTACTAGTTA GGACCAGACT 1500
TGGCATCGGC AACGATGTTG CAGGCCCTGG CGTGGGCCCT CTGGGCCTGA GCCCTCCTCG 1560
CAGCCCTGCG GGACCCCTCT GTCCCCCTTG AACACCACGT TCACCCAGCG TGGGTTCCTC 1620
TCCTCCCTGC CCTTCTGCCC CCGTCAGACC ACGGGACAGT CTCAGCCACG TCAGAGCCAG 1680
CATGGGCTCC CCACCACGCA GGCCTCCCTG CTTCTCCGGG CTTCTGCTTC TGTTACTATG 1740
ACGAGCTCCA CACTGCCCTC CCCCAGGAGG TCCCATCCTG CAGCCTGGTC TGCCCAGCTG 1800
GCTCCGGGGC GAGCGTGAGG GCCAGGCAGC TCAGCCCTCT AACACGTCTC TTCTCTTTTG 1860
ACCTCCTCAG 1870