EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS060-20783 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr2:219150830-219152460 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2382817chr2219151218hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:219151503-219151521GGAGGGAGGGATGGAAAG+6.31
SP2MA0516.2chr2:219152026-219152043CCCAGCCCCGCCCACTC+7.11
SP4MA0685.1chr2:219152027-219152044CCAGCCCCGCCCACTCT+6.41
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00326chr2:219145665-219158265Adipose_Nuclei
SE_03432chr2:219149789-219152314Brain_Angular_Gyrus
SE_06270chr2:219145735-219164206Brain_Hippocampus_Middle
SE_08985chr2:219150395-219151017Brain_Mid_Frontal_Lobe
SE_08985chr2:219151033-219151582Brain_Mid_Frontal_Lobe
SE_08985chr2:219151601-219152174Brain_Mid_Frontal_Lobe
SE_10092chr2:219146718-219159598CD14
SE_11206chr2:219145902-219159097CD20
SE_12180chr2:219148529-219157314CD3
SE_14014chr2:219148910-219157816CD34_Primary_RO01536
SE_15197chr2:219146865-219158111CD4_Memory_Primary_7pool
SE_16725chr2:219148483-219152907CD4_Naive_Primary_8pool
SE_17020chr2:219147008-219153025CD4p_CD225int_CD127p_Tmem
SE_17694chr2:219145927-219158488CD4p_CD25-_CD45RAp_Naive
SE_17933chr2:219145740-219158304CD4p_CD25-_CD45ROp_Memory
SE_18906chr2:219145938-219158335CD4p_CD25-_Il17-_PMAstim_Th
SE_19423chr2:219148822-219157978CD4p_CD25-_Il17p_PMAstim_Th17
SE_20197chr2:219147855-219154246CD56
SE_21204chr2:219148412-219158157CD8_Memory_7pool
SE_22529chr2:219146601-219158435CD8_primiary
SE_26022chr2:219146503-219160474Duodenum_Smooth_Muscle
SE_26969chr2:219146053-219152975Esophagus
SE_27658chr2:219148708-219161413Fetal_Intestine
SE_28578chr2:219146925-219161400Fetal_Intestine_Large
SE_30125chr2:219148759-219153194Fetal_Muscle
SE_32144chr2:219145915-219152965Gastric
SE_36018chr2:219146032-219158345HMEC
SE_41500chr2:219145847-219154222Left_Ventricle
SE_45286chr2:219149757-219152886NHLF
SE_47526chr2:219149905-219152925Pancreas
SE_50394chr2:219149842-219160653Sigmoid_Colon
SE_51585chr2:219145632-219158203Skeletal_Muscle
SE_52542chr2:219149722-219160735Small_Intestine
SE_57570chr2:219149965-219152053VACO_503
SE_57570chr2:219152277-219152769VACO_503
SE_58066chr2:219151254-219151909VACO_9m
SE_64537chr2:219148646-219152988NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2219151208219151930
Enhancer Sequence
CTAGAGGGGC TCACAGTCTG CAGGGACTTT AAGGTCCCCA CTGGAAGCCT GAATTTTCCC 60
AAAATACAGT AGGCATTCAC CTTCTGCTTG TTTTTGTTTT TCTTTTTGTT TTGGTAGAAA 120
CGGGGTTTCA CCATGTTGGC CAGGCTGGCA AACTCCTGGC CTCAAGTGAT CCACCCACCG 180
AGGCCTCCCA AAGTGCTGGG ATTACAGGCA TGAGCCACTG TGTCTGGCCC ACCTTCTGCT 240
TGAAGGAACT CCAGCAACAT GGAGCAAGCC CCTTGTCTGC AGACAGCTCG ATTAGAACAT 300
TCTTCCTTGC CTCACAATGC CTGTTATCAA GGCATTCAGA CTGTGCCCTA TCCTTGCCCA 360
TTATAGATCT AAGTTTGCTC CTCTCTCAGG GCCCCAGTCC CCCATTAGGA AGGAACCAGA 420
GCCCCTGCTT TCTACCACAG CAGCGGCACA AGTGGGTGAG CTCAGACAGC AGGACTTGCT 480
GGGTGTCAAG GTTTTCAGAT GCAGAGGCGG AAGCACCTCC TCCCCTGGAG CCCTCTCAGT 540
GTGGTAATCC TGCTGTCTGC CTACTGAGGC CCCGGCTGGG GCTCTCCTGG GGGTATTTGA 600
AGGGTTAAGG CTCCGGAATC TGCAGAGGAG GCCTGAGCTA CTGGGGTTAC AGCAAGAGGA 660
GAGTATGTGT ACTGGAGGGA GGGATGGAAA GGAGCAGCTG ACTGGTCCAG GCAGCCTGCC 720
CTCCTCCCTG CCAGAGACGG ATGCCCAGAG TGGAAAAAAA TAGCTCAGAA TGCACATCTC 780
AGGAAACCCC ACCCAGCAGG CGCAGGAGCA CAGCCCAGAT CTGACGATTT GTTCCCCTCC 840
CTTTTCCTTT ATCTGCCCCC ACAAGAAAAC ACTTTATCCT CCTACCCCAG GGCACAGCTG 900
ACCTCATAGC CACGAGAGCA AATGAGTAAA AAGATACACC CAGGAGTGTC TGGGCAAGTC 960
ACCAGGCCTG ATTCTGCACC AAGGGGGCCC AGAATCAACT AAATATCCTT CCATCAGCCT 1020
GGACTTTGGG ACTAAGAGGA TGAAGCCACA GGGATCTAAA CACTAAAATA TCAGAGCTGG 1080
CTTAGACTTT GGATCTCACC TGGTCATTTG ACAGACAAGG AAACCCCAGA GCCAAGAAAG 1140
TTCCTGCTCC ACCCCAGAAC AGCCCTCTTC TTCGTCATGG GTTTGGAACT TCCCTTCCCA 1200
GCCCCGCCCA CTCTCTGAGT GATAGACACC AGCACACACC CTCTCCCAAG GAGGGGCCAG 1260
AACAAGCTAC CATTCTCTCA GTTCTCTAGT GACCTCTCAG CTCAGAAACA GTTAAGACCG 1320
GGCCGGGTGC AGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGCAGGTGGA 1380
TCACGAGGTC AGGAGATCAA GACCATCGTG GCCAACATGG TCAAACCCCA TGTCTACTAA 1440
AAAATACAAA AAATTAGCTG GGCGTGATAT CCCACACCTG AAGTCCCAGC TACTCGGGAG 1500
GCTGAGGCAG GGGGATCGCT CGAACCCGAG AGGCAGAGGT TGCAGTGAGC CAAGAACATG 1560
CCATTGCACT CCAGCCTGGG CAACAAGAGT GAAACCCCAT CTCAAAAAAA AAGACAGCCA 1620
GCCCTCGACT 1630