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

TagContent
EnhancerAtlas ID
HS154-11536 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr19:45957860-45960710 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs8109532chr1945958294hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr19:45959150-45959161CTGAGTCACCC-6.02
IRF1MA0050.2chr19:45958311-45958332TCTTTCTTTCTTTTTTCTTTT+6.11
JUNBMA0490.1chr19:45959150-45959161CTGAGTCACCC-6.02
MYCMA0147.3chr19:45959266-45959278GGGCACGTGGCC-7.22
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_01498chr19:45958813-45960047Adrenal_Gland
SE_02108chr19:45958499-45960183Aorta
SE_02406chr19:45958430-45960350Astrocytes
SE_03036chr19:45958768-45959960Bladder
SE_06640chr19:45958730-45960254Brain_Hippocampus_Middle
SE_09930chr19:45956713-45960693CD14
SE_11261chr19:45958545-45960135CD20
SE_13038chr19:45958977-45959634CD34_Primary_RO01480
SE_14395chr19:45958713-45960104CD4_Memory_Primary_7pool
SE_19219chr19:45958648-45960125CD4p_CD25-_Il17p_PMAstim_Th17
SE_20014chr19:45958474-45960238CD56
SE_20748chr19:45959094-45960173CD8_Memory_7pool
SE_22333chr19:45958933-45959876CD8_primiary
SE_23143chr19:45958333-45960000Colon_Crypt_1
SE_23745chr19:45958435-45960006Colon_Crypt_2
SE_24769chr19:45958330-45960073Colon_Crypt_3
SE_26771chr19:45958314-45960076Esophagus
SE_29756chr19:45958492-45960156Fetal_Muscle
SE_31887chr19:45958242-45959952Gastric
SE_34472chr19:45958815-45960056HCT-116
SE_35967chr19:45958253-45960308HMEC
SE_38090chr19:45957862-45960688HUVEC
SE_39922chr19:45958724-45960027K562
SE_41239chr19:45958731-45960085Left_Ventricle
SE_44217chr19:45958500-45960314NHDF-Ad
SE_44830chr19:45958669-45960328NHLF
SE_45809chr19:45956766-45960850Osteoblasts
SE_47661chr19:45958698-45959895Pancreas
SE_48343chr19:45958657-45960059Psoas_Muscle
SE_49047chr19:45958609-45960056Right_Atrium
SE_50737chr19:45958444-45960123Sigmoid_Colon
SE_51420chr19:45958482-45960430Skeletal_Muscle
SE_52836chr19:45958420-45960076Small_Intestine
SE_53558chr19:45958651-45960115Spleen
SE_57973chr19:45958776-45959093VACO_9m
SE_57973chr19:45959154-45959797VACO_9m
SE_64393chr19:45958339-45960189NHEK
SE_65504chr19:45958083-45960176Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr194596059245960660
chr194595942045959846
Number: 1             
IDChromosomeStartEnd
GH19I045453chr194595637045960535
Enhancer Sequence
ACATGAGCTG TTTGGAGAGC TGCCTGGAGG AAGAGAAACC AGCCTGAGTT TCACAGGCTA 60
GTGGAATTTG GAGGGGGGCA ATAATAGCAA TAACAATAGG CCAGGCACGG TGGCTCACAC 120
CTGTAATCCC AGCACTTTGG GAGGCCGAGA AGGGTGGATC ACCTGAGGTC TGGAGTTCGA 180
GACCAGCCTG GCCAGCATGG CAAAACCCTG TCTTTACTAA AAATACAAAA AAAATTAACC 240
AGGCTTGGTG GTGTGTGCCT GTAATTCCAG CTACTCGGGA GGTTGAGGCA GGAGAATAAC 300
TTGAACCCGG GAGGTGTGGG TTGCAGTGAA CCGAGATCAT GCCACTGCAC TCCAGCCTGG 360
GCGACAGAGT GAGACTTTGT GTCAAAAACA ATAATAATAA TAATAATAAT GCACTAGGTG 420
CAGATACTGA TAAAGGCTTT GTGAGGAATT TTCTTTCTTT CTTTTTTCTT TTTTTTTTGA 480
GACAGAGTCT CACTCTCTTT CCTGGCTGGA GTGCAGTGGC ACGATCTCGG CTCACTGCAA 540
CCTCCGCCTC CCGGGTTCAA GCGATTCTCC TGCCTCAGGC TCCCAAGTGG CTGGGATAAC 600
AGGTGCCCAC CACTACGCCC AGCTAATTTT TTTTTTTTTT TTAGATAGGG TCTGGCTCTG 660
GCTCTGTCAT ACAGGCTGGA GCACAGTGGC ATGATGACAA CCCACTGCAG CCTTGACCTC 720
CTGGGCTTAA GTGATCCTCT TGCCTCAGCC TCCTGAGTAG CTGGGGCTAC AGGCTTATTT 780
TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT CTCAAACTTC TGGGCTCAAG 840
CAATCCTCCT GCCTTGGCTT CCCAAAGTGC TGGGTTTACA GGAGTGAGCC ACCATGTCTG 900
GCCATTTGAG GAAATTTTTA TTTTTGTCTG TCTTGTTTCC TGCTCTGTCC CCAGCACCTA 960
GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTAGGTG 1020
TGCTGATTAA ATATTTGAAT GGCTGATTGA ATGAACGAAT GAATGTCATC CTACAACCAC 1080
TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC TGGCCTCTGG GATCCCTCTT 1140
GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC TGAAGAGGGC GTGGAGGGGG 1200
CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC CTGGACAGCA GCCCAGAGTG 1260
TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC CTGAGTCACC CTGGGAGAAA CCCCAGCCAC 1320
ATACCTGGCC GCTGACATCA CCCGGCCAGG GCACCCCCGG CAGCCTAGAC AAGCTGACTG 1380
AATCACAGGC GGAATTCAGC CACCCCGGGC ACGTGGCCTG CTGTGACCCC CCGCAACACC 1440
CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG GCCGGGCACA CAGGGGTCAG TGAGGGGGCA 1500
TGGGGCCTGA GTCAGGGACA GGGTGGCTAC AGCCAGAGAC CACCCAGCCA CAGGCGTCCA 1560
TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT GGGGAGGCCC TGGCGGGTGA 1620
GGAGGAAGCA CGTGTGGGTG TGACGGGGAG GCTGCGGCTT GTGGGCAGCG GCTGGGCGAC 1680
CCACAGGGGT GGGATGGGGT CTGAGTGTTT GCGCAGAGAA TCACCAAATC GTAAGAGACT 1740
TGGTCGTAAG AGTCAGTCAG GAGGACAATG GAATCACCAA TGTGCTTACA CACGCAAAGG 1800
CACACACGCA CACTCAACAC CCGGCCTGGG GAGGCCCTGA CTCCACCCAC CCCAGGCCAG 1860
CGGGGCCTCA CTACCCATAA GCCTGCAAGT TCCCTAAGGG ACTGAGGCCT AAGGGACAGT 1920
TTCCTCATCT GTTGAGTGGG GGTATTAACA AGCATTATTA GGCCAGGCAC AGTGACTCGT 1980
GAGGCAGAGG TAGGCGGATC CCTTGGAGGC CAGAAGTTCA AGACCAGCCT GGACATCATA 2040
GCAAGACCCC TTCTCTACAA AGAAAAAATT TAAAAATTAG CTGGATGTGG TGGTGTGCAC 2100
CTGTAGTCCC AGGTACTCAG GAGGCTGTGG AGGGTGGATT GCTGGAGTGT TGGAGTTTGA 2160
GACTGCAGTG AGCTATTGAT TGCACCACTG TACTCCAGCC TAGACAACAG AACAAGATCC 2220
TATAGCAAAA AAAAAAAAAA AAAAAAATCA CTATTATTGT AATAGCTATG CTTACGGGGA 2280
ACATACTTTC TGCCAGGTGC TGTTCTAGGC ATTCTACATT TTTTTTTTTT AAATAATGGA 2340
GATGACGTCT CACTATGTTT CCCAGGCTGG TCTTGAACTC CTGAGCTCAG GCTATCCTCT 2400
CGCTTTTTTG GTGGCTGGCA CGCCTGTAAT CCCGACATTT TGGGAGGCCA AGGTGGGTGG 2460
ATCGCCGGAG CCCAAGAGTT CGAGACCAGC CTGGGAAACA TAGTGAGATG CCATCTCTAC 2520
CAAAAAATCA AAAAATTAGC TAAGCATGGT GGCTCATGCC TGTAGTCCCA GCTACTCAGG 2580
ATGCTGAGGT GGGAGGATCA CTTGAACCTG GGAGATGGAA GTTGCAGTAA GCTGAGATTG 2640
TGCCACTGCA CTCCAGCCTG GGTGACAGAA TAAGACCTTG TCTCAAAAAA AAAAAAAAAA 2700
AAAAAAAAAG AAGAAGAAAA AAGAGAGTCA ACTGCATCTG TATTTGTGGC ACTTGGTACA 2760
TACACGGTAA GCTTTCTCAA GTGACTCTGT TATGATTCTT AGTACTAAAC ATATTATTTT 2820
CCCTTTTTTT GTTTCTTTCT TTCTTTTTTT 2850