EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS056-10204 
Organism
Homo sapiens 
Tissue/cell
GC_B_cell 
Coordinate
chr21:45561920-45563080 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFKB1MA0105.4chr21:45562812-45562825TGGGGGTTCCCCT-6.05
Nkx2-5(var.2)MA0503.1chr21:45562845-45562856CTTGAGTGCCT-6.14
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00694chr21:45556304-45562174Adipose_Nuclei
SE_04775chr21:45562268-45567560Brain_Cingulate_Gyrus
SE_09453chr21:45561992-45566451CD14
SE_10160chr21:45556978-45567753CD19_Primary
SE_10883chr21:45549670-45568864CD20
SE_12057chr21:45561968-45566295CD3
SE_14927chr21:45557173-45566664CD4_Memory_Primary_7pool
SE_15569chr21:45562317-45566179CD4_Memory_Primary_8pool
SE_16226chr21:45559159-45566019CD4_Naive_Primary_7pool
SE_16681chr21:45562128-45566733CD4_Naive_Primary_8pool
SE_17033chr21:45557478-45566541CD4p_CD225int_CD127p_Tmem
SE_17488chr21:45556658-45567697CD4p_CD25-_CD45RAp_Naive
SE_17928chr21:45556798-45567404CD4p_CD25-_CD45ROp_Memory
SE_18688chr21:45556913-45567005CD4p_CD25-_Il17-_PMAstim_Th
SE_19210chr21:45556311-45566981CD4p_CD25-_Il17p_PMAstim_Th17
SE_20083chr21:45557255-45567673CD56
SE_22987chr21:45557144-45566653CD8_primiary
SE_24239chr21:45562136-45562596Colon_Crypt_2
SE_24239chr21:45562698-45564018Colon_Crypt_2
SE_31647chr21:45562800-45565120Gastric
SE_32667chr21:45562205-45567077GM12878
SE_40890chr21:45556355-45562047Left_Ventricle
SE_42286chr21:45556722-45566264Lung
SE_43630chr21:45562260-45568211MM1S
SE_50113chr21:45561874-45567505Sigmoid_Colon
SE_52463chr21:45562247-45566423Small_Intestine
SE_53405chr21:45552282-45566904Spleen
SE_55261chr21:45562152-45565145Thymus
SE_58720chr21:45552566-45596359Ly1
SE_59125chr21:45557380-45640832Ly3
SE_60477chr21:45556693-45597600DHL6
SE_61237chr21:45557180-45641526HBL1
SE_61527chr21:45545883-45641600Toledo
SE_62281chr21:45556124-45641130Tonsil
SE_65639chr21:45562160-45565153Pancreatic_islets
SE_67221chr21:45562260-45568211MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr214556214245562600
chr214556213145562483
Number: 2             
IDChromosomeStartEnd
GH21I044137chr214555689245567922
GH21I005115chr214555753345566332
Enhancer Sequence
GCAACCTCCG CCTCCCGGGG TCAAGCAATT CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA 60
TTACAGGTGT CTGCCACCAG GCCGAACTTT TGTAATTTTA ATAGAGACAA GTTTTCGCCA 120
TGTTAGTCAG GCTGGTCTCG AACTCCCGAC CTCAGGTGTT CTGCCTGCCT CAGCTGCCCA 180
AAGTGCTGGG ATTACAGGCA TGAGCCACTG CACCTGGCTG TGAAATGTGT TTTTAACAGT 240
GTTTCGTTAC AGCTCACGGT AGCAGTTTCC ACCTGGGCCT GTCGGGAGTG GGTAGGACTG 300
TAGACAGCGG GAGGAGGGAT GAAGGGTGCG GGGTGTTGAG GGCAGGGTGG GGCCTGACAG 360
CTGTGGGCTA CACCACAGGT TGCCAGGGGA TGGGGCTGCT GTTAATGAGG CCGTACTCCT 420
TCCACTGTTG CCCCTGGGTG GCCATGAGGC GCTGGACGAC ACAGGTCACT GAAGGCCCTG 480
CTGTGGGCAC AGTGCCTGGC ACACAGGGGC CTCTGTTGAC TTGGCAGGGA GGGGTTCCTG 540
ATGAAGCAGA AGCAGGTCCC AGGGGTGGGT GTGGCAGGAC CCTCAGTTTC AGGGCTGCTG 600
CGGCCTGTGC GTCAGGGTCA GGGGCGTGCG TCCACCAGCC TGCACTTGTT GAGAGTTGTG 660
CTGCAGGTCG GAGGCTGGCG AGGCTGCTCC TGGCCCGTTG TGCCTCCTGT AGAAGGGGGG 720
CTGGTGTGAA TGAGAAGTGC AGCTGTGTTA TCTATTGCTG GGTCACAGAC CACCCCACAA 780
CTCAGGGCTG GGGCAGCCGC ACATCATTAC CCTCTCTGTG AGTGGACTTT GGCAGCCCGG 840
GACTCTCGCC AGTCTGGGGT GTCCTGGGGC TTGGGGCTTA GCCCATGGCT GTTGGGGGTT 900
CCCCTCAGGG GTCCTTGGCC TGGTGCTTGA GTGCCTGCAG GGCGTGCTTG GCGGGGAGTG 960
GGGCTGAGGA CACCTCACTC TCAGCCTTGA GTCACCTGGT GCCACCTCCA TCACATCCCA 1020
TGGGCCACAG CCTTCTGGCA GCGCAGGCTC ACAGGGGGCA GGGTCGGCAG GGCTCCCGTG 1080
GCAGGGCAGC CTGGGGTCAT GGCGAGGGTA ATTTCTGTTC TGCAGGCCAT GCAGCCTGCC 1140
TGACCCGTGT TCTTTTCGCC 1160