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

TagContent
EnhancerAtlas ID
HS098-21641 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr16:31096580-31097280 
Target genes
Number: 39             
NameEnsembl ID
DCTPP1ENSG00000179958
SEPHS2ENSG00000179918
AC002310.10ENSG00000260494
AC002310.17ENSG00000261588
PRR14ENSG00000156858
SRCAPENSG00000080603
RP11ENSG00000261840
PHKG2ENSG00000156873
RNF40ENSG00000103549
MIR4519ENSG00000260083
BCL7CENSG00000099385
FBXL19ENSG00000099364
AC135048.13ENSG00000261487
ORAI3ENSG00000175938
SETD1AENSG00000099381
HSD3B7ENSG00000099377
STX1BENSG00000099365
STX4ENSG00000103496
AC135050.1ENSG00000232748
ZNF668ENSG00000167394
ZNF646ENSG00000167395
PRSS53ENSG00000151006
VKORC1ENSG00000167397
BCKDKENSG00000103507
AC135050.2ENSG00000252809
KAT8ENSG00000103510
PRSS36ENSG00000178226
FUSENSG00000089280
AC106782.18ENSG00000261359
PYCARDENSG00000103490
TRIM72ENSG00000177238
PYDC1ENSG00000169900
COX6A2ENSG00000156885
ARMC5ENSG00000140691
TGFB1I1ENSG00000140682
SLC5A2ENSG00000140675
C16orf58ENSG00000140688
CTDENSG00000261741
CSDAP1ENSG00000261614
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_37351chr16:31094578-31098520HSMMtube
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr163109682831097062
Number: 1             
IDChromosomeStartEnd
GH16I031084chr163109542031100082
Enhancer Sequence
GCTGAAACAG ATAAGTGCCT CATCTGACTT CTTGCTAAGC ACTTCCCACT TCCCATCAAA 60
TCCTCACAGT AGCTTTTGAA ATTGAATTTT GTTCCCCTCA TTACTGAAGG TAACCAAAGT 120
TCCAGAGAGG TTAAGAGACT TCCTTGCTCT GTAACTACAG GCAAGTGGCA GACTTGCGAT 180
TCGCAAGCCA GGGCCTGAGC TTTTAGCCCT GTTGGTCTGA TGGGACCCCT GTCCCAGCCT 240
CGTGGGAATG CCCCTACTTG TCACTCCCCT GCTCCACCCG TCTGCACCCT CCAGGATGGG 300
CCTGCCTCCC GTATTCCTGA CTCATTAGTG CATCTCTTAT CATCAAGACA TAATATCCGT 360
CCCAGGAATT ACTTTGCATT CAATTTGCAT GCCAGTCACT TAATGCCGGA ATTCTGACTG 420
GGAGCCCTAC CCTGTGCAGG CTCGCTGGGT CCCTGCTGGA AGCCTGCCAC TTCCCCAGAA 480
ACCCAAGTCA GGTCTCAGAG ATTCCTCTTC TCACCTAAAC TCCAAACCTG TAGAGTTCCA 540
AAGTGCCTGT GCCTCTCAGC CCTAACAGGG CTGTTCCCAT CCCAGGGGGT GAAAGAGCCC 600
CCTAATTAGG CTCGGCGGTG TGGATGCCTA TGCCAGTTCT CTAGTCCTAA CTGAGGTTTG 660
CTTCACAGTG GCTTCTGCCC ACTCCCAGCA TGCCCCACTC 700