EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS060-19084 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr2:43385260-43387000 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4952668chr243386568hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr2:43385486-43385507CCCTTCAGCTCCTCCTCCTCA-6.59
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_03102chr2:43384671-43387327Bladder
SE_09287chr2:43383934-43388379CD14
SE_10736chr2:43385270-43387369CD19_Primary
SE_11722chr2:43384536-43388438CD20
SE_11879chr2:43384841-43388354CD3
SE_14384chr2:43384968-43390226CD4_Memory_Primary_7pool
SE_16107chr2:43385039-43388515CD4_Naive_Primary_7pool
SE_16655chr2:43385030-43387619CD4_Naive_Primary_8pool
SE_16950chr2:43385153-43387343CD4p_CD225int_CD127p_Tmem
SE_17323chr2:43384367-43390308CD4p_CD25-_CD45RAp_Naive
SE_17875chr2:43384151-43389961CD4p_CD25-_CD45ROp_Memory
SE_18565chr2:43384470-43389555CD4p_CD25-_Il17-_PMAstim_Th
SE_19552chr2:43384838-43388407CD4p_CD25-_Il17p_PMAstim_Th17
SE_20209chr2:43384383-43388430CD56
SE_20901chr2:43385124-43387775CD8_Memory_7pool
SE_22349chr2:43384494-43388457CD8_primiary
SE_23059chr2:43384055-43387389Colon_Crypt_1
SE_23724chr2:43384477-43387342Colon_Crypt_2
SE_24685chr2:43384340-43387340Colon_Crypt_3
SE_25333chr2:43383856-43391948DND41
SE_26374chr2:43384543-43388739Duodenum_Smooth_Muscle
SE_26557chr2:43384020-43387372Esophagus
SE_27617chr2:43384083-43393474Fetal_Intestine
SE_28536chr2:43383866-43393674Fetal_Intestine_Large
SE_30898chr2:43384773-43387387Fetal_Thymus
SE_31392chr2:43384365-43391297Gastric
SE_34919chr2:43383855-43388500HeLa
SE_38828chr2:43385030-43386643HUVEC
SE_43203chr2:43384366-43387389Lung
SE_47826chr2:43384619-43386674Pancreas
SE_47826chr2:43386793-43387270Pancreas
SE_49954chr2:43384504-43386643RPMI-8402
SE_50052chr2:43384264-43393423Sigmoid_Colon
SE_52337chr2:43383845-43392633Small_Intestine
SE_53288chr2:43384755-43387396Spleen
SE_55101chr2:43384949-43387332Thymus
SE_56731chr2:43384774-43386703VACO_400
SE_56731chr2:43386712-43387326VACO_400
SE_58412chr2:43352450-43425007Ly1
SE_61450chr2:43354337-43468354Toledo
SE_62203chr2:43354169-43468733Tonsil
SE_65350chr2:43384329-43388234Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr24338547743386677
chr24338593843386506
Number: 1             
IDChromosomeStartEnd
GH02I043156chr24338374143393336
Enhancer Sequence
AGGTCTCCAC CAGCTGCTGA GCACAGCGGA GGTGGGGAGG CAAGAGCATG TCCTATCCTG 60
CCTCCTGGCC CCCAGCCCCA GTAACACAGA ACTAGGGTGC CTATTGTTTC AATGGCAGAA 120
ATCCCCCTCC CCTCCGACCC CTGCCCCCTG CAGCACTGCT CCCCATCACT GGGCTAAACG 180
AATGACCCGC CACTCAGCAG GTGACGACTT ACTCCTCCTT GGCCGGCCCT TCAGCTCCTC 240
CTCCTCACCC ATCCTGACTC AGAGGCCTGT CAGCTGCCAC TGCCCCCGAG GCCTGGCAGA 300
TTTGGGTGGG AAGGAGCTAT CTGGGTGCCA GGACCTGAGG GGCTGGCCAT GCCCTCACTC 360
CTTACTGACC TGACCTTTAG CAGGGCCTCT GAGCATTCTC TGATCTAGAA ATGCCACATG 420
TACACGCATG TGTGTGCACA CACACACAAA CACCCACACA CTCACACCCA GCCGCTCTAT 480
GACCTGATGA AACAGTCTGG GTGCAGGGCT GAGGCAGGCC AGGGAGGAGA GTTAGACTGA 540
GCAAAAGCAG GATGTGTGTG GAGCAGCCTC CTGGCCTCTC TCCCGCAGAG GCACTTCCTG 600
GTACTGGAGG GCAAAGCGGC CCGGGGTTGG GAAAGAGACC GGTGCTGCTT GCTCCCTCTC 660
CAGAACAGGC ATTAATTCTG GCTGCCCCTT GGTATTGGCC TCCAACTTTA TAGTTCTCTC 720
CCTTTCTTTC TCTCTCTCTC TCCTACACAC ACCCCTCTAG ACTCCTCCCC TGCACCTCCT 780
CAAAATTTCT CACCCACCCT CACCCCACAG AAGGAGCATC AAAGCCCCAC ATAGCCTCTG 840
GCCTCTCTCA ACACCTAGGA GTTGAGATCA GGCCCTTGTG GCCCAGTCTT GGGGACTTCC 900
CCCTACCAGG GTTGGCCCTC TTGGGTCCAC GCCTCTTTGG CTAGACTTCT GATCGCTCTG 960
GCGGCCACTC CGCAGTTTCA CCACGCCTGC TCCTGCCTGC AACACACAGA AGTTGGCAGT 1020
GACTCTGCAC TGCTCCCAGC ACCCCGGATG GCTCAGGGCT GTGGCATTTT GTTTTCTTTC 1080
GTTTTTCGCC TTCATGTCTG TGCTGTTCAC TGTGCCTGAA ATCCCCTCCC CGCTAACCCT 1140
CCTGCCCATA GCGTCAGTGG CCCACATGTC AGCACCCAGC ACTTACCACT AGCGAGGCTG 1200
TGTCCTATCC TCCTGACCAT GCCAATGAAA AAAGTCCCAT TAATTATACC CACTGTTGGC 1260
CGGGTGCGAT GGCTCTCACC TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGAAGGATCA 1320
CTTGAGCTCA GGAGTTCAAG ACCAGCCTGG GCAACATGGC AAGCCCCATC TCTACAAACA 1380
ATGCAAAAAT TAGCCGGGTG TGGTGGCGTG CACCTGTAGT CCCAGTCCCA GCTACTTGGG 1440
AGGCTGAGGT GGGAGGATCA CTGGAGCCCT GGAGGTGGAG GTTGCTGTGA GCTGAGATCA 1500
CGCCACTGCA CTCCAGCCTG GGCAACTGAG GGACCTTGTC TCAAAAAAAA AAAAAAAAAA 1560
AAGATACCAT TGTTCAGAGG AGGAAGCTGA GCTGACAGAG GTCAAGGAAG ATGCATTTCT 1620
ACCCAGCTTT CAAGATTCAC TTTGGACATC ACCTTCCTCA GACTCTGCCT TCTCCTCTTC 1680
ACCGCCCCAC TACGCCCCAG GCAGGAGAAA CTGCTCCCAG CCTAGAGCCA CTGCCCGTTG 1740