EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-21430 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr21:44201310-44202760 
TF binding sites/motifs
Number: 33             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr21:44202102-44202120CCTTCCTCCTCTCCCTCC-6.05
EWSR1-FLI1MA0149.1chr21:44202174-44202192CCTTTCTCCCCTCCCTCC-6.05
EWSR1-FLI1MA0149.1chr21:44202059-44202077CCTCCCTCCCCTCTTTCC-6.09
EWSR1-FLI1MA0149.1chr21:44202129-44202147CCTCCCTCCCCTCCCTCC-6.09
EWSR1-FLI1MA0149.1chr21:44202147-44202165TCTGCCTCCCTTCCCTCC-6.41
EWSR1-FLI1MA0149.1chr21:44202032-44202050CCTGCCTCCCCTCCCTCC-6.4
EsrraMA0592.2chr21:44202255-44202266ATGACCTTGAG-6.02
EsrrgMA0643.1chr21:44202255-44202265ATGACCTTGA-6.02
Myod1MA0499.1chr21:44202285-44202298AGGAGCAGCTGCA-6.15
Nr5a2MA0505.1chr21:44202254-44202269CATGACCTTGAGCTT-6.83
ZNF263MA0528.1chr21:44202098-44202119CTCCCCTTCCTCCTCTCCCTC-6.05
ZNF263MA0528.1chr21:44202179-44202200CTCCCCTCCCTCCCCTCACTC-6.12
ZNF263MA0528.1chr21:44202082-44202103CTCCCCTCCCTCCCCTCTCCC-6.17
ZNF263MA0528.1chr21:44202089-44202110CCCTCCCCTCTCCCCTTCCTC-6.17
ZNF263MA0528.1chr21:44202077-44202098CGTCCCTCCCCTCCCTCCCCT-6.31
ZNF263MA0528.1chr21:44202138-44202159CCTCCCTCCTCTGCCTCCCTT-6.36
ZNF263MA0528.1chr21:44202037-44202058CTCCCCTCCCTCCCCTGCCTC-6.45
ZNF263MA0528.1chr21:44202096-44202117CTCTCCCCTTCCTCCTCTCCC-6.45
ZNF263MA0528.1chr21:44202120-44202141TCTTACTCCCCTCCCTCCCCT-6.5
ZNF263MA0528.1chr21:44202135-44202156TCCCCTCCCTCCTCTGCCTCC-6.5
ZNF263MA0528.1chr21:44202111-44202132TCTCCCTCCTCTTACTCCCCT-6.61
ZNF263MA0528.1chr21:44202043-44202064TCCCTCCCCTGCCTCTCCTCC-6.64
ZNF263MA0528.1chr21:44202055-44202076CTCTCCTCCCTCCCCTCTTTC-6.6
ZNF263MA0528.1chr21:44202046-44202067CTCCCCTGCCTCTCCTCCCTC-6.78
ZNF263MA0528.1chr21:44202170-44202191CTCTCCTTTCTCCCCTCCCTC-6.84
ZNF263MA0528.1chr21:44202152-44202173CTCCCTTCCCTCCCCTGCCTC-6
ZNF263MA0528.1chr21:44202219-44202240TCTCCCTCTCCTCTCTCCTCT-7.08
ZNF263MA0528.1chr21:44202174-44202195CCTTTCTCCCCTCCCTCCCCT-7.23
ZNF263MA0528.1chr21:44202125-44202146CTCCCCTCCCTCCCCTCCCTC-7.53
ZNF263MA0528.1chr21:44202090-44202111CCTCCCCTCTCCCCTTCCTCC-7.76
ZNF263MA0528.1chr21:44202093-44202114CCCCTCTCCCCTTCCTCCTCT-8.48
ZNF263MA0528.1chr21:44202129-44202150CCTCCCTCCCCTCCCTCCTCT-8.74
ZNF263MA0528.1chr21:44202102-44202123CCTTCCTCCTCTCCCTCCTCT-8.99
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr214420160044202012
chr214420145044202500
Number: 1             
IDChromosomeStartEnd
GH21I042780chr214420106144202826
Enhancer Sequence
GGAAAACAAG GTGAGCTGCC GCCTTGGACA CCCTCCTCTT AATTCTGGTT CCTTCCTGCT 60
CGACATGGGG ACGGGACAGT CCGACGCTCC CTCTCATGGG AATGTATTTG CAGACATCAT 120
ATCATGGAAA ATACTAAACA CAAGTGTTGC CTCAGAAGCT CACGATGAGC CGGGTTCACG 180
CCGGTGTAAT TCTGCGGGGG CCGGACCCTG AATCTCATGC ACGCGCGGCT GCGAAGGCGA 240
CGCAGCTTCT GCCTCTGAGC CGCCTCCTTC GATACATCCC GTGGGAGCGG GAGCCACACT 300
GAGCGCCAGG TCTGCGGCCA GCCGGGTGGG AAACAGGCGC TGCTGCCAGC AAGCTCCTCC 360
CACTCTGCTC ACCTGCCCCG AGGTTCCCAG AAGTTCTCAA TCAGTACCAT GTCCTTTCCC 420
CTTCTCGAAG AAAAACACTG TTGGCAATGG AACAGCGCAT CCCATTATCC TCCTGTCTTC 480
ACCAGGAACA GGCTCCCCAG ACAGCAGACA CTGTTTTCCG CGAGCCGGAG GCAGCCAGAT 540
TTGAGCCCAG ATACCGCCAT GGCCACTCCT GCGAAACCCT AGAAAGCCAG GGACATATTC 600
AGGGGACTTC TCTTGCTCCA AGAAGCCGTG CCTGGCAGTC AGCGCCTGCA CACAGGCAGC 660
TCCCATGGCA GGAGCATGGG TGGCCAAAGG GGCCAAGGTT CTCTGTTGTC AGTCCTGCCT 720
CGCCTGCCTC CCCTCCCTCC CCTGCCTCTC CTCCCTCCCC TCTTTCCCGT CCCTCCCCTC 780
CCTCCCCTCT CCCCTTCCTC CTCTCCCTCC TCTTACTCCC CTCCCTCCCC TCCCTCCTCT 840
GCCTCCCTTC CCTCCCCTGC CTCTCCTTTC TCCCCTCCCT CCCCTCACTC CCTTCCCTCT 900
CTTTCCTTCT CTCCCTCTCC TCTCTCCTCT CCCTTCCCTG CCTGCATGAC CTTGAGCTTT 960
TCCTCTGTTA GTCCCAGGAG CAGCTGCACT GGGTCAGGAG TTTCTGAGCC TGGCTGGTCC 1020
TCAGGCCGTC TGTGGACACT GAGACACGCC CCAGCCCTGA GATTCTGATT CTGTAGGCCT 1080
GTTCTGGTTG CCAGGTCTGT TTTGCCAAGC TGTGTGTTTC TGGTGCAAGG CGTAGGGTGC 1140
GCGCTCGATG GCCTCCTGGG TGCTGCCATC TGCCCATCTG TATCTGCATC TGATGCCCGT 1200
GAGGAGACAT AATGGAAGCA AGAGTGTGGG GTGGGAGGCC CTAATTGTTT CAGGGAAGTG 1260
TCCCAGCTTG GAAGTGGATT CTTGCAGGGG CTCTGGTCTG GTGGAGAAAG TGGAGAAGGC 1320
AGCCTGGGGA CGTGGCTGGG TGGGGAGTGG GCGCAGGCAC AGAGCCAGCC TGCATGCTCC 1380
TTCTCTCCCT CCATGGACAT AAGGACAGTG AAGTACTGTC CATACCACCG CGTCCAGGCA 1440
TCTCACACGC 1450