EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-23041 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr2:219150970-219152390 
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: 35             
IDCoordinateTissue/cell
SE_00326chr2:219145665-219158265Adipose_Nuclei
SE_03432chr2:219149789-219152314Brain_Angular_Gyrus
SE_06270chr2:219145735-219164206Brain_Hippocampus_Middle
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_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
CAGGCTGGCA AACTCCTGGC CTCAAGTGAT CCACCCACCG AGGCCTCCCA AAGTGCTGGG 60
ATTACAGGCA TGAGCCACTG TGTCTGGCCC ACCTTCTGCT TGAAGGAACT CCAGCAACAT 120
GGAGCAAGCC CCTTGTCTGC AGACAGCTCG ATTAGAACAT TCTTCCTTGC CTCACAATGC 180
CTGTTATCAA GGCATTCAGA CTGTGCCCTA TCCTTGCCCA TTATAGATCT AAGTTTGCTC 240
CTCTCTCAGG GCCCCAGTCC CCCATTAGGA AGGAACCAGA GCCCCTGCTT TCTACCACAG 300
CAGCGGCACA AGTGGGTGAG CTCAGACAGC AGGACTTGCT GGGTGTCAAG GTTTTCAGAT 360
GCAGAGGCGG AAGCACCTCC TCCCCTGGAG CCCTCTCAGT GTGGTAATCC TGCTGTCTGC 420
CTACTGAGGC CCCGGCTGGG GCTCTCCTGG GGGTATTTGA AGGGTTAAGG CTCCGGAATC 480
TGCAGAGGAG GCCTGAGCTA CTGGGGTTAC AGCAAGAGGA GAGTATGTGT ACTGGAGGGA 540
GGGATGGAAA GGAGCAGCTG ACTGGTCCAG GCAGCCTGCC CTCCTCCCTG CCAGAGACGG 600
ATGCCCAGAG TGGAAAAAAA TAGCTCAGAA TGCACATCTC AGGAAACCCC ACCCAGCAGG 660
CGCAGGAGCA CAGCCCAGAT CTGACGATTT GTTCCCCTCC CTTTTCCTTT ATCTGCCCCC 720
ACAAGAAAAC ACTTTATCCT CCTACCCCAG GGCACAGCTG ACCTCATAGC CACGAGAGCA 780
AATGAGTAAA AAGATACACC CAGGAGTGTC TGGGCAAGTC ACCAGGCCTG ATTCTGCACC 840
AAGGGGGCCC AGAATCAACT AAATATCCTT CCATCAGCCT GGACTTTGGG ACTAAGAGGA 900
TGAAGCCACA GGGATCTAAA CACTAAAATA TCAGAGCTGG CTTAGACTTT GGATCTCACC 960
TGGTCATTTG ACAGACAAGG AAACCCCAGA GCCAAGAAAG TTCCTGCTCC ACCCCAGAAC 1020
AGCCCTCTTC TTCGTCATGG GTTTGGAACT TCCCTTCCCA GCCCCGCCCA CTCTCTGAGT 1080
GATAGACACC AGCACACACC CTCTCCCAAG GAGGGGCCAG AACAAGCTAC CATTCTCTCA 1140
GTTCTCTAGT GACCTCTCAG CTCAGAAACA GTTAAGACCG GGCCGGGTGC AGTGGCTCAT 1200
GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGCAGGTGGA TCACGAGGTC AGGAGATCAA 1260
GACCATCGTG GCCAACATGG TCAAACCCCA TGTCTACTAA AAAATACAAA AAATTAGCTG 1320
GGCGTGATAT CCCACACCTG AAGTCCCAGC TACTCGGGAG GCTGAGGCAG GGGGATCGCT 1380
CGAACCCGAG AGGCAGAGGT TGCAGTGAGC CAAGAACATG 1420