EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS030-10294 
Organism
Homo sapiens 
Tissue/cell
CyT49 
Coordinate
chr2:219150220-219152760 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2382817chr2219151218hg19
TF binding sites/motifs
Number: 5             
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
ZNF263MA0528.1chr2:219150745-219150766AGGGAAGGAGGGAGAAGGGGA+6.27
ZNF263MA0528.1chr2:219150748-219150769GAAGGAGGGAGAAGGGGAGAG+8.31
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00326chr2:219145665-219158265Adipose_Nuclei
SE_03432chr2:219149789-219152314Brain_Angular_Gyrus
SE_03432chr2:219152339-219152890Brain_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_08985chr2:219152421-219152794Brain_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_58066chr2:219152411-219152693VACO_9m
SE_64537chr2:219148646-219152988NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr2219152622219152760
chr2219151208219151930
Enhancer Sequence
GCCTGGCCAA CGGCCCCAGG AGAAGAGGGT GGCCCAGGCT TGGAGATACA TAAAGGTCAG 60
AGCTGGAAAG AAACTCACCC AAGGACAGCC AACCCCTCAC TTTACCAACT AGACAGCCAC 120
AGCACAGGAA CCTGTCCTTG GTTACCGAGC TGGTCCTGGG GACAGGACGA GATCCTAGCT 180
GTCTACATAG AGAGACCTGG GCACAGGAGA GGAAACCCCA GCATTAACGC TAGCCAGGGG 240
AGTTGCTAAA CTCAGCCACA CTCACCTCTG AGCAGTGCCA AGAACACTGT CAGACTGGCA 300
AGAGCCTCCG GGGACCAGGG CTGCCGGGTT TGGCAGCTTT AGAGCCTGCT CTTGGGCTTC 360
TGCCCAGCCT CCATGAGGGC CCTGGCCACT TCCACATCAG CAAGGCCTCC ACTAGGGATG 420
AGGTTTGGGG CTGGCATCTG CCTAGGTAGC AGCAAAGGGG GAAAGGGTCA GTGTTTACTT 480
TCGTAGCTAT GTCTAAGGGT GGAGGCTAGA GAAGAATGGA GGGTAAGGGA AGGAGGGAGA 540
AGGGGAGAGA GATCACGAGA CTGACACAGA GTGAGGACTA GAAATCAGAT CTGGGTTCTG 600
CCAGCAGCTA CTAGAGGGGC TCACAGTCTG CAGGGACTTT AAGGTCCCCA CTGGAAGCCT 660
GAATTTTCCC AAAATACAGT AGGCATTCAC CTTCTGCTTG TTTTTGTTTT TCTTTTTGTT 720
TTGGTAGAAA CGGGGTTTCA CCATGTTGGC CAGGCTGGCA AACTCCTGGC CTCAAGTGAT 780
CCACCCACCG AGGCCTCCCA AAGTGCTGGG ATTACAGGCA TGAGCCACTG TGTCTGGCCC 840
ACCTTCTGCT TGAAGGAACT CCAGCAACAT GGAGCAAGCC CCTTGTCTGC AGACAGCTCG 900
ATTAGAACAT TCTTCCTTGC CTCACAATGC CTGTTATCAA GGCATTCAGA CTGTGCCCTA 960
TCCTTGCCCA TTATAGATCT AAGTTTGCTC CTCTCTCAGG GCCCCAGTCC CCCATTAGGA 1020
AGGAACCAGA GCCCCTGCTT TCTACCACAG CAGCGGCACA AGTGGGTGAG CTCAGACAGC 1080
AGGACTTGCT GGGTGTCAAG GTTTTCAGAT GCAGAGGCGG AAGCACCTCC TCCCCTGGAG 1140
CCCTCTCAGT GTGGTAATCC TGCTGTCTGC CTACTGAGGC CCCGGCTGGG GCTCTCCTGG 1200
GGGTATTTGA AGGGTTAAGG CTCCGGAATC TGCAGAGGAG GCCTGAGCTA CTGGGGTTAC 1260
AGCAAGAGGA GAGTATGTGT ACTGGAGGGA GGGATGGAAA GGAGCAGCTG ACTGGTCCAG 1320
GCAGCCTGCC CTCCTCCCTG CCAGAGACGG ATGCCCAGAG TGGAAAAAAA TAGCTCAGAA 1380
TGCACATCTC AGGAAACCCC ACCCAGCAGG CGCAGGAGCA CAGCCCAGAT CTGACGATTT 1440
GTTCCCCTCC CTTTTCCTTT ATCTGCCCCC ACAAGAAAAC ACTTTATCCT CCTACCCCAG 1500
GGCACAGCTG ACCTCATAGC CACGAGAGCA AATGAGTAAA AAGATACACC CAGGAGTGTC 1560
TGGGCAAGTC ACCAGGCCTG ATTCTGCACC AAGGGGGCCC AGAATCAACT AAATATCCTT 1620
CCATCAGCCT GGACTTTGGG ACTAAGAGGA TGAAGCCACA GGGATCTAAA CACTAAAATA 1680
TCAGAGCTGG CTTAGACTTT GGATCTCACC TGGTCATTTG ACAGACAAGG AAACCCCAGA 1740
GCCAAGAAAG TTCCTGCTCC ACCCCAGAAC AGCCCTCTTC TTCGTCATGG GTTTGGAACT 1800
TCCCTTCCCA GCCCCGCCCA CTCTCTGAGT GATAGACACC AGCACACACC CTCTCCCAAG 1860
GAGGGGCCAG AACAAGCTAC CATTCTCTCA GTTCTCTAGT GACCTCTCAG CTCAGAAACA 1920
GTTAAGACCG GGCCGGGTGC AGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCCGA 1980
GGCAGGTGGA TCACGAGGTC AGGAGATCAA GACCATCGTG GCCAACATGG TCAAACCCCA 2040
TGTCTACTAA AAAATACAAA AAATTAGCTG GGCGTGATAT CCCACACCTG AAGTCCCAGC 2100
TACTCGGGAG GCTGAGGCAG GGGGATCGCT CGAACCCGAG AGGCAGAGGT TGCAGTGAGC 2160
CAAGAACATG CCATTGCACT CCAGCCTGGG CAACAAGAGT GAAACCCCAT CTCAAAAAAA 2220
AAGACAGCCA GCCCTCGACT TCTGGCCCCC AACTCGAGGC CACCCCTCCC AGCCCCCTCT 2280
CTAGCCAGGG TGGCCTCTCT CTGGACCCAT GGAGACCGAG GGGTGGCTCC AAGCTCCCAG 2340
GAGGGAGAGG CTGTCCTGGG GATCACGAGA GGACCCAGGC ACCGCAGCTC CGCCACCCTT 2400
GTCTGGAGCA GAATCCTGTG ATCAGAATGG TAATCTCGGG TTACCCCACC CAAGTCAGGA 2460
TGGCCTGGGA GTACAGATAA GGGAAGAGGA AGCCATTAGC AGGCTGATGC TATAATACTT 2520
CTGAGCACAG TCCCTGTTCA 2540