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

EnhancerAtlas 2.0

Tag

Content

EnhancerAtlas ID

HS139-11668

Organism

Homo sapiens

Tissue/cell

Myotube

Coordinate

chr12:7242840-7244040

Target genes

Number: 31
Name	Ensembl ID

MRPL51	ENSG00000111639
SCARNA10	ENSG00000239002
GAPDH	ENSG00000111640
ING4	ENSG00000111653
COPS7A	ENSG00000111652
PTMS	ENSG00000159335
MLF2	ENSG00000089693
LEPREL2	ENSG00000110811
CDCA3	ENSG00000111665
USP5	ENSG00000111667
TPI1	ENSG00000111669
RPL13P5	ENSG00000240370
LRRC23	ENSG00000010626
SPSB2	ENSG00000111671
ENO2	ENSG00000111674
ATN1	ENSG00000111676
C12orf57	ENSG00000111678
PTPN6	ENSG00000111679
SCARNA12	ENSG00000238795
EMG1	ENSG00000126749
PHB2	ENSG00000215021
U47924.19	ENSG00000255896
C1S	ENSG00000182326
LPCAT3	ENSG00000111684
RP3	ENSG00000257078
C1R	ENSG00000159403
ABC12	ENSG00000205885
C1RL	ENSG00000139178
RBP5	ENSG00000139194
CLSTN3	ENSG00000139182
PEX5	ENSG00000139197

HEDD

Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome	Start	End

chr12

7242922

7243105

Enhancer Sequence

AGATCTGGTG GAAGAAGGAC AGGGGGTAGG AAGAAGATCT GTTGCGGAGT GGCGCACGTG 60
GTGGCTCAGT GATGGTCCTC CTTGTCTCGC CCAGAGTGCA TCATGCACCA CAATGGCTCT 120
GGCTGGTCAC TACCTGCTGG GCTCAGCTGC TGCAAACTTC CCCATGTGAC TTTCAGCTGT 180
TCCCTGAGTC TCCCACTGAC TCACTCTTTG CGTGTTGTCC TGGACTGGGT ACCTCACCCT 240
TTCCCTGTTT TCTGCTCCTC TGGCAGGTTT CAGGTCCTTC TCCATCCCCA CCACCTCCTA 300
TGGCCTGTTC CCCTGGGGTC CTGGTTGTCT GTACCCAGCC TTTACCTGCC CCTCATTCCC 360
AGAGCTCAGA CAGCTCCGCT TTATTTTCTG TCTTCAGATT CCACCTCAGC CTAATCAAAC 420
CATTCACACC TCGAGTGCCT CCTGATGCCC TCGGCGGAAC ATGAGCCCTG AAGCCCACCC 480
ATCTCAGTGT CAGCAGGCAC TGCCTCGTCC CTCTTCCTTC CTCCTCACAG CCTCCTCAAC 540
CTCTCCTTGA CTCTGCCAGC AAACGCCCTC CCCCAACACT GCACACTCGC CAAGTCTTCT 600
GAGCCGGTAA GACGTGCCAT TGTCATGTAA TTCACGCATA ATCTCCAGGG GTCTCCTGGG 660
AATGGTAGTT GTTGGACCTT CGCAGGCTCT GCTTGAGCCC TGAATCTCAT TTTTACTGGA 720
TAGAGAAAGA CAGGCCTGGG AAGGTACCCT TGGTTGCCAC AGAGGTGAGG GTTCTGAGCA 780
CACTGTCCTT GCTGAAGGCT ATTCCTGTGC TGCCAGAGCC CACATTTCTC CTCCTCATGT 840
CCCTGTGTTC CTGTTGAAGC AGGCAGCCAT GTCAATCATT TCCTTGGAGA CAGGGAAGCT 900
GAGGCACAGT GGTTTCCCAA AGACTCTCAG CTAGACAGCA GATGGGGAAG GTTTTCCTGA 960
CTCAGTGGAT GTTGAATTTC CTGAGTGGGT CCTGTCCCCT TCCTTCTCTG TGCTTCTCCC 1020
CTCAGTGCTC ACCGAGGGCC TCTACACCAG TGAGCGCCCA TCCAGGGCAT CCCCGGGCTC 1080
TCAGAGAGGC CGTTGGCCAT CAGCTCTTGT GGGGCTGGGC TGTGTCTGGG GGTGTGCATG 1140
CCATACAGAT CCCAGATCCC AGAGGGCCCA GTTTTGTCTC CCCTCTGCCC GCCCATCCTG 1200