EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS091-21211 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:74270320-74271890 
Target genes
Number: 40             
NameEnsembl ID
KIAA0195ENSG00000177728
CASKIN2ENSG00000177303
TSEN54ENSG00000182173
C17orf110ENSG00000259120
RECQL5ENSG00000108469
SAP30BPENSG00000161526
ITGB4ENSG00000132470
GALK1ENSG00000108479
H3F3BENSG00000132475
UNKENSG00000132478
UNC13DENSG00000092929
WBP2ENSG00000132471
TRIM47ENSG00000132481
TRIM65ENSG00000141569
MRPL38ENSG00000204316
FBF1ENSG00000188878
TEN1ENSG00000257949
RP11ENSG00000261408
ACOX1ENSG00000161533
CDK3ENSG00000250506
EVPLENSG00000167880
SRP68ENSG00000167881
GALR2ENSG00000182687
ZACNENSG00000186919
ATF4P3ENSG00000228218
RNF157ENSG00000141576
FAM100BENSG00000185262
QRICH2ENSG00000129646
SPHK1ENSG00000176170
PRPSAP1ENSG00000161542
UBE2OENSG00000175931
AANATENSG00000129673
RHBDF2ENSG00000129667
CYGBENSG00000161544
AC090699.1ENSG00000163597
ST6GALNAC2ENSG00000070731
ST6GALNAC1ENSG00000070526
MXRA7ENSG00000182534
JMJD6ENSG00000070495
SRSF2ENSG00000161547
Number of super-enhancer constituents: 18             
IDCoordinateTissue/cell
SE_10428chr17:74261317-74270738CD19_Primary
SE_10428chr17:74271353-74272367CD19_Primary
SE_11415chr17:74257434-74273567CD20
SE_18937chr17:74270190-74271331CD4p_CD25-_Il17-_PMAstim_Th
SE_23599chr17:74270231-74271001Colon_Crypt_1
SE_24931chr17:74269202-74271077Colon_Crypt_3
SE_24931chr17:74271333-74272189Colon_Crypt_3
SE_27367chr17:74270135-74270940Esophagus
SE_31864chr17:74264958-74270935Gastric
SE_43246chr17:74266783-74271643Lung
SE_48284chr17:74258480-74271528Psoas_Muscle
SE_52552chr17:74270088-74271032Small_Intestine
SE_53757chr17:74270122-74270832Spleen
SE_58966chr17:74257592-74273389Ly3
SE_60322chr17:74239092-74270751Ly4
SE_60510chr17:74247565-74275632DHL6
SE_61026chr17:74257641-74276199HBL1
SE_62440chr17:74241844-74272934Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177427170174271846
Enhancer Sequence
CTTTCTGTTG ACGAGAAGAA ACTGTAAGAC AGGGGTGCTG AGGTTGCTCA ACACATTCCC 60
CAAGCCCACC AGGGGTCACC CCAGCCTGCC CAATGCCCAG GGAGGTTGAG AGCAGTTCTG 120
TTCGCCATGC TGGGCTGACA CAGGCTGGAG GGGAGCTGCC GGGGCCGGGG GGCACGGCGC 180
AGGCCCATCT GAGCTCCTAA GCAGTCATGA AGCACCCTTC ATGATCTTGT GAATGAAAAA 240
TAAGCAAACA CGTCCTTCTG CAGGAGCCAA GAGCTGCCTC TTTGGTACTG TTTCCTGTTA 300
ATACAGACAC GAGGTGACAT CCACACCAAC AGGCACAGGA ATTTTCCTGA GACTACCAGT 360
CCCTCTCTCC TGCTTCCAGG GCATTTTCAG TGCCCTTAGA GTAGACACTG GGAGAAGGGA 420
GCTAAGTATT CCCAAGAAAA CAGAGTTCTG GGAGCCAGGG TGACAGTCAT GTGCTCACTG 480
TCCACCACTG AGACCTGCCG TTCCCAGCAC AGCCTCTGGG CCAGAGGGCT TGGCTTTGAA 540
CTCCAGCTCT GCCGCTTCCT GGCTGTGTGA CCTAGAGCAA GGACCTTCAC CTCTCTGTGC 600
CTCAGTTTTC TCAGCTGTAA GTGGTGCTAA CGGCCCCTAC CTCTAAGTGC TGGTACATAG 660
ATTGAAAGTG GTTCGTCCAT GTAAAGCTCC TAAACTACCT GGTCTGTGGG GGGCCCTGGA 720
TGATGCTGAG GAGCCATGAG CACCGCAGCC ACTTTTCTGT TGTGATTTCC TCCTCCCTCA 780
GCGCCGGGTC CTCACTGAGG GCTGGAGTGA TGCTGGAGAG CATCTAGCCG AGGGGCAGGG 840
GAGGGTGGAG GCTCTGGTTG GGGAGGGTCC CTGAACCTCC CACAGACATT CACAAGGAAT 900
GTGGGTGCAT AACTGTTTTA CAGGAGGAAG GTCGGCAGCT TTTATTAGAT TCTTGGGGGG 960
GGCCTGACTC CAAGCAGCAC TAACCCAGCA CCCCCTTGAT GACAGACGAG GAAACTGAGG 1020
TCTGGAGAGG GGAGAGCCCT TGTCAAGAGT GACCTTGCCC AGGGTCACTT GTCAGTGATC 1080
CAGCCTCCTG GCTGCAGGGC CTTGTTACCA AACCCTCCTG ACCTTCAGGC CCAACTTAGC 1140
TCCTGCGGAG ATCAAGGACC CAAGGGATCT TCCAGGCGGG AGGCAGAGAG AGGTTCCTCC 1200
ATGACAGGGT CGTGGCCTCT TGGGGACCCG GGCATGGCCT GTGCCCAGCA GCCACCATGC 1260
AGAGCCCAGG CGCACGAGCT CCATGACAGT GAGTGCACGT GAGCAGGGCA AGGGCATGGA 1320
CCTGGAGCCA GAGATGTGGG TGGTGACCCT GTCCCTATTT CATCTTCTGT GGAATGGGAC 1380
AGTAACAGCA CCTACCCACC TCCCAGAAGG GGCACAAATC ACTCAGTCAC TCGGGGTTCC 1440
TCTTTTCCAC ACCCATCCCC CCCTTCGGCT CCCAGGCCCT CCCCTCTCCG GGGAGATAAA 1500
GGCCCTACAT GAGCAGGAAA GGGGGCCGGC AGGGCCAGCG GGGAGGCCTG GCAGGACGCC 1560
CCACCCAGAG 1570