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

TagContent
EnhancerAtlas ID
HS041-00563 
Organism
Homo sapiens 
Tissue/cell
EWS502 
Coordinate
chr1:21664280-21666490 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CrxMA0467.1chr1:21666141-21666152CTAATCCCCTT-6.32
Nr2f6MA0677.1chr1:21665975-21665989TGACCTTTGAGCCT-6.37
RxraMA0512.2chr1:21665975-21665989TGACCTTTGAGCCT-6.14
ZNF263MA0528.1chr1:21664550-21664571CCCCTCTGCCCTCCCTCATCC-6.55
ZNF263MA0528.1chr1:21664532-21664553CCTTCCTTCCCCTTCTGCCCC-6.58
ZNF263MA0528.1chr1:21665441-21665462GGAGGAGGATGGGGAGAGGAG+8.11
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00105chr1:21656775-21671990Adipose_Nuclei
SE_00854chr1:21663168-21667245Adrenal_Gland
SE_01643chr1:21663301-21667219Aorta
SE_02944chr1:21664000-21666080Bladder
SE_02944chr1:21666135-21667266Bladder
SE_04518chr1:21663353-21665909Brain_Anterior_Caudate
SE_05710chr1:21664624-21665800Brain_Cingulate_Gyrus
SE_05944chr1:21659989-21673592Brain_Hippocampus_Middle
SE_08398chr1:21663323-21665931Brain_Inferior_Temporal_Lobe
SE_26127chr1:21663680-21666771Duodenum_Smooth_Muscle
SE_26770chr1:21663415-21667226Esophagus
SE_28486chr1:21663392-21666819Fetal_Intestine
SE_29337chr1:21663370-21667087Fetal_Intestine_Large
SE_31433chr1:21663236-21672659Gastric
SE_39164chr1:21663441-21666942IMR90
SE_42174chr1:21663299-21667069Lung
SE_45045chr1:21663454-21666210NHLF
SE_46660chr1:21664031-21667287Ovary
SE_47592chr1:21663572-21665292Pancreas
SE_47592chr1:21665303-21666898Pancreas
SE_48583chr1:21663300-21667219Right_Atrium
SE_50108chr1:21663357-21673470Sigmoid_Colon
SE_52633chr1:21663378-21667298Small_Intestine
SE_53334chr1:21663536-21666469Spleen
SE_54639chr1:21663094-21674002Stomach_Smooth_Muscle
SE_56171chr1:21663474-21665484u87
SE_65263chr1:21660486-21671744Pancreatic_islets
SE_67931chr1:21663474-21665484u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12166440021664833
chr12166494721665143
Enhancer Sequence
CTGTCCAAGG TGACAATGCA AAAAGTGAGG ATGCCAGGTT TGAACCTGGG CCCATCAGTC 60
TCCAAGGCCC ACTCCTGCTG CACGGGCAGA TCCCGCCTCC CTGCCCTCTC CTCCCCACAC 120
TGCCTGCTCA GATGTGGCAC CTGGAGGCAG CCAGTCCTCG CCCCTCGCCC CCTCCTCTCC 180
AGTGCTGGAA GGAACAGCTC ATGTGTGTAA TGGACTCGAA GCTTCTGTGA AAGAGCTGCT 240
GAGGAAATGA GTCCTTCCTT CCCCTTCTGC CCCCTCTGCC CTCCCTCATC CCTCTCATGG 300
CCACATAGCT CTGAGGACAT TTCAGCCCTG GACCTCCGCC CAATAAGAAG GGACTCCAAT 360
GGCCAGGCAG CTGGGGGTGT GTGTGGTATT GACCAAGGAG CTTTCTCAAC CCCTGGACAC 420
CCCAGCCCAG CCTGTGGCCT CTCAGAGGAC CAGGAGGACA TGAGGTTAGA GTCCCCACCC 480
TTGGCTCCAG TTTCCAAGTG ACGCAACCAA GTGTCTGGAT TCAGAGAATC GCAAAATGTT 540
TATCTGGAAT CACAACCACC ACCATGACCA TTTAATCAAA CCTTATCCTG TGCCAAGTGC 600
TACAAACATA GCTCATGAAT CCTCACCAGC AAACAAAATG GGTACTGCTA GGCTCTCATT 660
TTACAGAGGA AGAAAGTGGA GCTCAAAGGG GTTAGGTGCC TTGCCCCAAG TCTCACAGTG 720
AGGAAGTGGT GGGGCTGGAA TTCAAACCCA GATTTGCACA ACTTCGAGTC TATCCTCTGA 780
ATGAGAGTAT TATACTTGTC ATCCTGCATG TCATTACTGA AGACGGCCCT GGAGTCAGTC 840
TGCTCCAGCC ATGTCATTTC ACAGATGGGA AGACTGAGGC CCACGAAGGA AGACCGTGGT 900
TCAGGAGGAC AAGGATTAGT GGCAGAGCCT GGGCTGGAAG CCACCCTGGC CTTGCTTTCA 960
ATGACCAGAT CAGAGCCTGG GAGCGGGCCA TGTGCAGCTG GATGGGCAGC TGGAGGGAGT 1020
CAGGCAGGGA GGTGGGAGGC TCTGCTTCCA GGCAGAGGTA AATATTGACA TGACTGTGTT 1080
TACGCTGTAA CCTAACTCTG CCTGGCTGCT GCCCCAGGCC CACCCTCCTG CCTTCCCAGC 1140
CAAGGAGGGA AGGGAGCTGT GGGAGGAGGA TGGGGAGAGG AGGCTTCTGG GCCAGGGGCT 1200
GCTCCTCCTG CTTAGAGGGC TATGTGGTCA GAAAGGCTGG GACATCAGGT GTTAGGGGTG 1260
GGGGTTAGTG GAGACCCAGG CCAGGGGACC AGGTGGTGCC AGACAGGGAG GGGCTGTTAT 1320
CTGAGCTGGG GAGCTGGGGA TCTCAGGGCG GGGGACTGGG CTGGGAGTCA CAAGGCCTGA 1380
GTTCAAGTTC TAGTTCTGCT ACTGATTGGC AGTGGGAATC CAAGAACAGT CGGTGAATGG 1440
GGAAGAAAAG GTCTAACTGT CAAGTGCGGT GCAAAGGTGA ACAATAAATA ACCAGCATTT 1500
GAGCCTGGCC AGTGTCCAGC CCCAGTGAGC TCTCAACGCC TCTGGCTACC GGCTCAACAG 1560
TCCTATCCCT GTCCCAGTGG GCTTTCCCAG GAAGGCCAAG TTTCTGCCAA ACTGAGTGGC 1620
AGCTTGGGAC TGAAGCCATA ATAATCTAGA GGAATCGGGG AGCCACTGTC TAGCTCCCGT 1680
CCCTAATTCC CTAAGTGACC TTTGAGCCTC AGCTTTTACA ACTCTGAAAT AAGGCTCACC 1740
CTCCTCCCTG GGGTTGGTGT GAAGAGCAGA GATTACATTT AAGTGCCAGG CACATAGTAG 1800
ATGCTCATTT TGTCTCTCAG TCTTCCCACT TGTCAAACAG GGGCCTCGAA GTTGGTGGTT 1860
CCTAATCCCC TTTTCATACA AGCGCTCTAG CGTCTTTAGA AGGCCCAGAA GCCAGGCCCA 1920
CCTCCCTGAT GTTAGATCCC CACCTAGCCG ATTTCCTGAA TGCTCTCTAG AAACTTGCTC 1980
CCCTGTTTAC ACCTCCCCCC AGGAAGTCCA AAGGGGCCCT GTTGGGAGGA GGGAGCCATT 2040
CCTAGGCTTG TCAGCCCACC AAGACAGGCC TGGGGCATCC CAGCCACTCT GCCCTCAGGG 2100
GCCCAAGGAA AGGGCAGGCC CCAGGTCCTG GACTCCAGTG CCACCCTGAC AGTGGGGTTC 2160
CGCCAGCACT GGTTGTTCAT TAAACTGTGC CCCTCAGACT ATTAACTCTT 2210