EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS056-10208 
Organism
Homo sapiens 
Tissue/cell
GC_B_cell 
Coordinate
chr21:45615240-45617360 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs762421chr2145615561hg19
rs7282490chr2145615741hg19
rs4456788chr2145616324hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SPI1MA0080.4chr21:45616347-45616361TGCTTCCTCTTTTC-6
SPICMA0687.1chr21:45616347-45616361TGCTTCCTCTTTTC-6.1
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00694chr21:45616149-45617521Adipose_Nuclei
SE_03880chr21:45616016-45617515Brain_Anterior_Caudate
SE_04775chr21:45609944-45617953Brain_Cingulate_Gyrus
SE_05779chr21:45610164-45618120Brain_Hippocampus_Middle
SE_06690chr21:45610194-45617897Brain_Hippocampus_Middle_150
SE_07737chr21:45615485-45617603Brain_Inferior_Temporal_Lobe
SE_10305chr21:45615103-45617503CD19_Primary
SE_11616chr21:45614519-45618143CD20
SE_24239chr21:45615918-45616296Colon_Crypt_2
SE_24239chr21:45616358-45616947Colon_Crypt_2
SE_30176chr21:45612703-45617986Fetal_Muscle
SE_31647chr21:45615831-45617002Gastric
SE_31647chr21:45617022-45617833Gastric
SE_33667chr21:45611717-45615585H2171
SE_40890chr21:45610212-45615559Left_Ventricle
SE_40890chr21:45615577-45618069Left_Ventricle
SE_42286chr21:45615697-45617796Lung
SE_48538chr21:45614456-45617946Psoas_Muscle
SE_50113chr21:45612958-45615570Sigmoid_Colon
SE_50113chr21:45615772-45617519Sigmoid_Colon
SE_51445chr21:45609930-45618288Skeletal_Muscle
SE_52463chr21:45612982-45615536Small_Intestine
SE_52463chr21:45615642-45617687Small_Intestine
SE_59125chr21:45557380-45640832Ly3
SE_61237chr21:45557180-45641526HBL1
SE_61527chr21:45545883-45641600Toledo
SE_62281chr21:45556124-45641130Tonsil
SE_65639chr21:45615968-45617001Pancreatic_islets
SE_65639chr21:45617003-45617940Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr214561565445615733
chr214561563545617233
Number: 2             
IDChromosomeStartEnd
GH21I005064chr214561583045617229
GH21I044192chr214561202445617843
Enhancer Sequence
GAAGCCCCCG CCCTGCCAAG GAATGTCACG AGCCTCAAGC AGATTTGCTC TTAGATATTT 60
CTTTTTAATC GAGTCTAACA GTGATTGTTG AGCCGTCCTT CATTTTTTTT TTTTTTTGTA 120
AGATGCCTCT GTCAAGAAGG AGCCACGAGT TGGCTTTCAT GGAATGGGTG CTCTTGGTGG 180
CCAAATAGAA ATAAAACCTG GCTGTCTGGT CCTGATCCAC TCACAGAAGT GGCGTAAACA 240
CCTTATTTAT GATCTGGGAC ATTCAACACC ATCTTATAAA AGATTCATAG AATACACATT 300
CACACACCCA CAAAAATCAA GAGAGCAGAT TTTCCAAAAA TAGGTGCAAG AAAGATCCAA 360
CTTCCAGGAT AAAATTTTAG AACCAACATT TCCATTAGCA AAAGCGGTCT TGTCTAAAAC 420
TCTACCGACC GCGCTAAAAT CCCATTCAAA ACAGAGCTCT GGTTACGTAG ATCGTGATCA 480
ATAATGAGAA ACTGTGAGGC GTCCCCGTGG GATCTGACAC TTCCTAGGGG AGCTTCTCTC 540
CACTGGTAAT AAAGATATAA TTAGGAATTT CAACTACCTG TGATTTTGCC AACTTACGGC 600
ATTTGTTGAG AATTTCGGTC CCTGTGTTTA TGCACACACC TTTCAACCTT AGATTTGACG 660
GTGATGGGTT AGTAAATGTC AATTCTAAAG TGGTCGTTTT CAACCAGGGG CAATTTTACC 720
CCTCAGGGGA CACTGGCAGT GTCTGGAGAC ATGTTTGGTT GTCATGACTT GGGGCAGAGG 780
TGCCACGGGC ACCTGGAGGG TGGAGGCCGG GGTGCGGCTC AATACCCTAA CCACACAGGA 840
TGGCCCCAGG ACAAAGATGC CCCTGGTGCT GAGAGCAGGG CCCTGTTCTA AGAGATGGGT 900
GGCTGGAGCC TGGCTGGAGG GCACTAGTGG CACTCTGGGC TGGTCTCCCA GGGCCCCATC 960
TGCCAGGTCG GGGGCCCACG TGGGCCTGCA GGATGTGCGT GCTTCTCTGC TGTTGAGATT 1020
GCATCAGCAC AACAGCCACA GCCGTGACAC GGGGGCAGGC ACCTCAGTGA CGCCAGAGTC 1080
GGGGCGGGAG GTGTGGAGAT CTGGGCTTGC TTCCTCTTTT CAGTCCCAGG ACAGCTCCTC 1140
TTTGGCTGTG GGAGGCCCAG CTTCAGCCTT GTCTGTGGCT TCCTGGTGGG AGGACACAGG 1200
CCTTGAGGGA CGTTTGTCCG AGACGGTCCT CATCCTACTG GTAGGGACAC AGAGCACCTG 1260
TTCCTCTGGC CCCTCCAGGA GCAAGACACA TGCACTGCTG AGGCCTTGGA AGCCTACACA 1320
GGTTTATCAC CCACGGCCAG ACCTGTCTGT CAGGGAGCAG GTGGGGTCAT CCTGCCCTGA 1380
AGCACCGATG AGCTGATCCC GGTCATGCAG AGTGGGTGGG GACCTCTTGG CTGGGCCTGT 1440
TCATGTAGCA CACACGGCTT TGCTGCCCAT AGAATCCAGG GCCCCCAGTG TGAGCACCAC 1500
TCTCCATCCC TGAGGCCGAG CCTTACCCTG GAGGCAGCCT CAGGTGAGAT GCCCCTAATG 1560
GAGCCACCTG GCAATGGACC GCTCTCAGGT CCTTCAGCTC GGTGCACTCA CCCGGGAGCC 1620
CTGCGTTCTG TCCTGGGGTA GAGGCTCAGG GTTGGTTTGA AGCCATATAG TCAGCTCCCA 1680
GAGTCACAGA AACGTCCAAG GAAGAAAACT GTCCGATTAC AGACTTTTAA AATTCATTCA 1740
TAGTTTAATC AAGAGAACTT GCTGTTCCTT CCTCAAATTT CCTAGAATTG GTCTTCTCAT 1800
AATCACCACC TAGGGCACAG CTGTGGCCGA GGCTCCCATG ATGAAGCGTC TGTGTCAGCG 1860
CTGACGAGGT CTGCCGAGGA CGCGTTTCTC TCTGCAGCCC GGCACCAGTC TCAAGGCCAT 1920
CGGCTCCGAC AGCGTCACCT CCTGGGACCT TCCCTTCATG TATGGTCCCA GCGGCATGCG 1980
GGCCTGGTGG AGGAGGTCCT GGCCTGCCGC CCAGGGATGG CCGGTCCAGG CGCAGGGCCG 2040
ATTGTCCACT TCTGGCCCCT GAGGTACCGG GAGGGCTGGT GAGCAGCATG TCTCGCTCTG 2100
AGACCGGCCA GGCTGCTGGG 2120