EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS154-12257 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr2:43384740-43387350 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4952668chr243386568hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TCF7L2MA0523.1chr2:43384789-43384803AAAGTTCAAAGGCA+6.63
ZNF263MA0528.1chr2:43387224-43387245CCCTCCTACTCACCCACCTCC-6.02
ZNF263MA0528.1chr2:43384747-43384768CTTCCCTGCCACCCCTGCTCC-6.12
ZNF263MA0528.1chr2:43385486-43385507CCCTTCAGCTCCTCCTCCTCA-6.59
ZNF263MA0528.1chr2:43387208-43387229TCCTCCTTTTTCTCCTCCCTC-7.66
ZNF263MA0528.1chr2:43387205-43387226CCCTCCTCCTTTTTCTCCTCC-8.51
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
GCCTGTCCTT CCCTGCCACC CCTGCTCCGC CCCAGGCCAG CATTCCTGGA AAGTTCAAAG 60
GCACTTGGTT CAGGGGAGAT GTTTCCACAC AGCTTCTGTA GCTGGAACTG GGCTAGGCAG 120
AGAGGGGGCC CACCCACAGC CCCACAGGGA CTGCATCTTG AGACCAGAAA ACTTGGAGTG 180
GCCCTGGGGG AGCAGTGCTG TTCCCATTCT CTGTGGCAGG GGCCTTGGCA GGTGCAAGAC 240
CCAGAGTGTC CCCCCACAAC CTGAGGGGGC TGCTTCTGGA CACAGAGAGC TCAGGCCTCA 300
AATGCATCTT TTCACTAGCC TTCCTGGGTC CTGCCCATTC CTAGAGACGG AGTTCACTAT 360
GCTCCTAGCC ATGTGCTGGG TGCGGGGCGA GCCCCAGATG GCTCATCGCC ACGAGGTGCA 420
GGCACAGCCT CTCCATGAGC CATCAGGAAC TCGGGGTTGC ATCAAATCCC CAAAGACTTT 480
ACTGGGCCCA CGCTAGGCAT CAGCCTGGGA TTCTCCTCCC AGGTCTCCAC CAGCTGCTGA 540
GCACAGCGGA GGTGGGGAGG CAAGAGCATG TCCTATCCTG CCTCCTGGCC CCCAGCCCCA 600
GTAACACAGA ACTAGGGTGC CTATTGTTTC AATGGCAGAA ATCCCCCTCC CCTCCGACCC 660
CTGCCCCCTG CAGCACTGCT CCCCATCACT GGGCTAAACG AATGACCCGC CACTCAGCAG 720
GTGACGACTT ACTCCTCCTT GGCCGGCCCT TCAGCTCCTC CTCCTCACCC ATCCTGACTC 780
AGAGGCCTGT CAGCTGCCAC TGCCCCCGAG GCCTGGCAGA TTTGGGTGGG AAGGAGCTAT 840
CTGGGTGCCA GGACCTGAGG GGCTGGCCAT GCCCTCACTC CTTACTGACC TGACCTTTAG 900
CAGGGCCTCT GAGCATTCTC TGATCTAGAA ATGCCACATG TACACGCATG TGTGTGCACA 960
CACACACAAA CACCCACACA CTCACACCCA GCCGCTCTAT GACCTGATGA AACAGTCTGG 1020
GTGCAGGGCT GAGGCAGGCC AGGGAGGAGA GTTAGACTGA GCAAAAGCAG GATGTGTGTG 1080
GAGCAGCCTC CTGGCCTCTC TCCCGCAGAG GCACTTCCTG GTACTGGAGG GCAAAGCGGC 1140
CCGGGGTTGG GAAAGAGACC GGTGCTGCTT GCTCCCTCTC CAGAACAGGC ATTAATTCTG 1200
GCTGCCCCTT GGTATTGGCC TCCAACTTTA TAGTTCTCTC CCTTTCTTTC TCTCTCTCTC 1260
TCCTACACAC ACCCCTCTAG ACTCCTCCCC TGCACCTCCT CAAAATTTCT CACCCACCCT 1320
CACCCCACAG AAGGAGCATC AAAGCCCCAC ATAGCCTCTG GCCTCTCTCA ACACCTAGGA 1380
GTTGAGATCA GGCCCTTGTG GCCCAGTCTT GGGGACTTCC CCCTACCAGG GTTGGCCCTC 1440
TTGGGTCCAC GCCTCTTTGG CTAGACTTCT GATCGCTCTG GCGGCCACTC CGCAGTTTCA 1500
CCACGCCTGC TCCTGCCTGC AACACACAGA AGTTGGCAGT GACTCTGCAC TGCTCCCAGC 1560
ACCCCGGATG GCTCAGGGCT GTGGCATTTT GTTTTCTTTC GTTTTTCGCC TTCATGTCTG 1620
TGCTGTTCAC TGTGCCTGAA ATCCCCTCCC CGCTAACCCT CCTGCCCATA GCGTCAGTGG 1680
CCCACATGTC AGCACCCAGC ACTTACCACT AGCGAGGCTG TGTCCTATCC TCCTGACCAT 1740
GCCAATGAAA AAAGTCCCAT TAATTATACC CACTGTTGGC CGGGTGCGAT GGCTCTCACC 1800
TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGAAGGATCA CTTGAGCTCA GGAGTTCAAG 1860
ACCAGCCTGG GCAACATGGC AAGCCCCATC TCTACAAACA ATGCAAAAAT TAGCCGGGTG 1920
TGGTGGCGTG CACCTGTAGT CCCAGTCCCA GCTACTTGGG AGGCTGAGGT GGGAGGATCA 1980
CTGGAGCCCT GGAGGTGGAG GTTGCTGTGA GCTGAGATCA CGCCACTGCA CTCCAGCCTG 2040
GGCAACTGAG GGACCTTGTC TCAAAAAAAA AAAAAAAAAA AAGATACCAT TGTTCAGAGG 2100
AGGAAGCTGA GCTGACAGAG GTCAAGGAAG ATGCATTTCT ACCCAGCTTT CAAGATTCAC 2160
TTTGGACATC ACCTTCCTCA GACTCTGCCT TCTCCTCTTC ACCGCCCCAC TACGCCCCAG 2220
GCAGGAGAAA CTGCTCCCAG CCTAGAGCCA CTGCCCGTTG TAGTGACTTC TGTTTGAGGC 2280
TGAGACCTCA GCCCCCAGGT CCTGATTTGT GCCCTCCTCC CTCAGTTTTG GGGCCTGTGA 2340
GAGTGGGTGG CTGGGCCTGG GGCTGAGTCA CTGCCTAGCC TTGCCTGCCC AGCCCCGAAC 2400
CAGGCAAGCC TCGGTGCAGG TGACCCTGCT GCCCAGAGAA GTGGGCGGCA GGAAGAATGG 2460
TCAGGCCCTC CTCCTTTTTC TCCTCCCTCC TACTCACCCA CCTCCTGGCC ACTTTCCTCC 2520
CTTTTTTTTC TTTTTTTGAG ATGGAGTCTC ACTCTGTCGC CCACACTGCA GTGCAGTGGC 2580
ACAATCTTGG CTCACTGCAA CCTCTGCCTC 2610