EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS060-13579 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr16:84629610-84632290 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr16:84632252-84632272CTCCCCCCCAACCCCCCCCA+6.15
RREB1MA0073.1chr16:84632262-84632282ACCCCCCCCACCAACCCCGA+6.33
RREB1MA0073.1chr16:84632265-84632285CCCCCCACCAACCCCGACCT+6.33
RREB1MA0073.1chr16:84632255-84632275CCCCCCAACCCCCCCCACCA+6.57
RREB1MA0073.1chr16:84632256-84632276CCCCCAACCCCCCCCACCAA+6.66
ZNF263MA0528.1chr16:84631226-84631247AGAGGAAGAGGTGGAGAAGAG+6.26
ZNF263MA0528.1chr16:84632238-84632259CTCCTCCTCCCCTTCTCCCCC-6.32
ZNF740MA0753.2chr16:84632260-84632273CAACCCCCCCCAC+6.5
Number of super-enhancer constituents: 22             
IDCoordinateTissue/cell
SE_09246chr16:84625458-84646481CD14
SE_10600chr16:84629515-84636021CD19_Primary
SE_11114chr16:84621939-84652116CD20
SE_12322chr16:84630364-84636136CD3
SE_14767chr16:84627217-84632267CD4_Memory_Primary_7pool
SE_15740chr16:84630504-84632150CD4_Memory_Primary_8pool
SE_16608chr16:84630166-84632235CD4_Naive_Primary_8pool
SE_17292chr16:84630276-84632295CD4p_CD225int_CD127p_Tmem
SE_18003chr16:84625951-84646438CD4p_CD25-_CD45ROp_Memory
SE_18985chr16:84625856-84637709CD4p_CD25-_Il17-_PMAstim_Th
SE_19809chr16:84627254-84636010CD4p_CD25-_Il17p_PMAstim_Th17
SE_21255chr16:84630216-84632217CD8_Memory_7pool
SE_31867chr16:84627346-84635991Gastric
SE_32646chr16:84626311-84630293GM12878
SE_32646chr16:84630635-84632341GM12878
SE_53279chr16:84629459-84632344Small_Intestine
SE_53428chr16:84629488-84645031Spleen
SE_58632chr16:84618716-84691095Ly1
SE_59422chr16:84582392-84644442Ly3
SE_60919chr16:84626327-84654674DHL6
SE_61298chr16:84618328-84643462HBL1
SE_62422chr16:84609550-84652864Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr168463158384631836
chr168463091284631735
chr168463116084631348
Number: 1             
IDChromosomeStartEnd
GH16I084592chr168462626184644894
Enhancer Sequence
CTGCCCAGAA GAAGGTTGGT ACCTGGGCTT TCCATCACCC TCACTGTGCC ACTTGGTCCC 60
CAACAGGGCC AATGGTCCAT CTCTTCAAAC TGAAGCTGAG AGTCCAGGTC TACGCAGAGG 120
AGACAGGGAG ACTGGGCAAC CCCAGTGGGG GACGGGGGAC CCAGGACTTC ACCCAAACAC 180
AGGTACCAGA GACAGATGCC ATGAGCTCCT TCTGCTGGAG CCCTCAGCAC AGGGGAGTGG 240
TCTATACCCT TAACCTTCTC TGCAATGTCC AGGGTGCAAG TTCAAATTCC AGAATCCTTT 300
AGAAACTTAC CCCCACATGT ACTAGCCTTG TGACCCAGCC CAGAGTCCTG AATGTCTCTA 360
AGCCTCAGTT TCCTCATCCA CAAAATGGGT CAAATACTTA CCTCATAAAG TGGTTGGGAG 420
GATTACATGA AAAAGAAATG AGATCTGAAG GGTTGGCTGA TGGGAATCAT TGCTGATTTT 480
TGACCCCCAA CACCTCTCCA GTGAAACTGC CCTCAGGGGT CCACAGGGGC CTCCTAATTG 540
CCAAAGCCAA CAGCATCTTC TCCATGCCCA CTGGTGGCGT TTCACGCCAT TATCAATTCT 600
GCCCTCCTTG AACCTCTCCC TTCCCACGGC ACCCAGGGCA TGGTGCCATC TTGGTTCTCA 660
GAGCACTGAT CCCGCCTTCT ACTTTCTCCC CGGCTCTTCC ACCCCCTCTG TCTCCACACA 720
CACACTCCCC AGGGTTCCAC CTCATCCTCT CCTTTCCCCT GACACTCTCT CCCTGGGAGA 780
TCTCAGCTAC CACCACAGAA CACTGACGCA CCAGCCCCTG CCCTCACAAC TCTCCACTGC 840
TCTGTCCTTA ACAAGGTGGA CAGAGTCTGC CCTCTGTTTC TCGCCATTTC CTGGCACCTC 900
GCACCCCTTA CACACAACTG TTCGCTAAGG CAATCTGGAG CACTTAGAAG AGCACAAACT 960
CCAGAGATCA GCCAGCCAGG GCCGCATCCC AGCCAGGGCC GCATCCTAGC AGGGGCCGCA 1020
TCCCAGCCGG CTTCCTTCTA GCTATGGAAC ATCAGATGAG GGTGCTTCAT GCTCTGAGCC 1080
TCAGCTGTTC CAGCTGTAGA ATGGGGACCA CTTTCTGCAT CCAGCTCTGG GTTTCAGAGT 1140
GAGGCACTCC GAGGCACACA GTCACGGAGT CACTCCTTCT GTGAGTCTTT CTTGAGGAGA 1200
GATGGAAGAC AGTGAAGGTC TGAGAGGTAA CTGAGCCCCA AGTCTACTAA GCACTTATGA 1260
GGGGCCAGTC CCCACTCTAA GAATCTGCAC ACTGCAGATT CTTCTCCTCT GTGAGGGCAG 1320
CACAGATCGC AGTCCCATTT CACAGATGAA GAAACTGAGG CTTGGAGAGG TGAAGTGAGA 1380
ATGAGCCACA CAATTCTCCC TGCCCGCTGC AGAGCTGCTG AAGTCCACAG CAGCAGTTCT 1440
CAAAGTGTGG TCCTCGGACC AGCAGCACCA CAGCACCCGG GAACTTATTA GAAATGTGGG 1500
TACTCAGGCT CCACTCAGCC CTACTGATCC AGACGCTGGG AGTGGAGCTC TGAAACTGTG 1560
CTCGAATGAG CCCCAGGGTG ATTCTGAGGC TGCCAAACCT TGAGACCCAC TGACTTAGAG 1620
GAAGAGGTGG AGAAGAGGAA ATGGTGAGAA CTCACTGTTG GGAGAGGGGA CGAGACAAAG 1680
GTCTCAAGGA CAGAAAAGCT GAAGTGCTCA GAGTTCAGCC CCCACGCCCT CCTTGCTGCC 1740
TGTCTGCCTT TTATTTTAAG CAAATGACTG CATGAAGCAG CTTCCTGCAG AGTCCGTGGT 1800
TCCTGAGCAC GCCCATCAAA GACCACCAGG ACAGTCCCTC CAGTGCTCCC TCCCCAAAAT 1860
CCCACACCCC AAGAGAGGGA ACAGCCATCA TTAGCAAGAG AGCTACTGAC TATCAGCCCT 1920
GGGTACCAGG AGGCCTTTCT GCCTGTGCTG CCTCTAGCTC CTCTGCTTGC CCATAAGCCA 1980
CGAGGATTCA GATGCATATC ATAGCATCAC ACTGAGCCCC ATCTCAGGGC TGCCGTCACT 2040
GAGGATACAG CAAGGTCAGG AGCCCCATCC TGAGGACGGT GGTTTCCTTC TGGTCGGTGT 2100
CATGCACTCA GAGCCCAGGC CAATTGCACG CTGGATGTCC CTGATTTGAA GACTATGGAT 2160
GCCCTCCCCT TCCCACCCAG AGAGAGTCTT GTTCATGAAA AGACACAGCT GTTATGTTTA 2220
ACGTTAATAA AACTTCACTC TCAAAAGAGC CGGACCCTTC CTTCCACTGG TCTATGAAGC 2280
CTCATCAGAA GCCAATGATG GAGCTTTGGC TCCTGCAAAG GACCCGTGGG GACCTAGAAG 2340
CCCCAGGCAG GGCCCTGAAG GTAGGTAAAG GGAGCCTCAG TCCAATGCCC AGGTCATCTC 2400
TTCAAGGTTC TCTGCCTTCA TTTACTAAGT AAGTTCATCT GTGTCAACAA ATCAGCATCC 2460
TAACGTTCTC AGGATACCGC CTGGCGCAGA GCTGTGAACT CAGCAGCCGG CCCTGGTGGC 2520
TGTTACATGC TCTTTTCTCT GGCCTTTCCC TCTCCTGGCT CTCCTCTGAC CTTTCCCCTG 2580
GGTCCTGGAG GTGCCTTTAC GCCTCTCCCA CCTCCTCCCC ATCTGTGCCT CCTCCTCCCC 2640
TTCTCCCCCC CAACCCCCCC CACCAACCCC GACCTCTCTG 2680