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

TagContent
EnhancerAtlas ID
HS020-22846 
Organism
Homo sapiens 
Tissue/cell
CD34+ 
Coordinate
chr19:45958070-45960540 
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: 39             
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_47661chr19:45958424-45958684Pancreas
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: 1             
ChromosomeStartEnd
chr194595942045959846
Number: 1             
IDChromosomeStartEnd
GH19I045453chr194595637045960535
Enhancer Sequence
TCTTTACTAA AAATACAAAA AAAATTAACC AGGCTTGGTG GTGTGTGCCT GTAATTCCAG 60
CTACTCGGGA GGTTGAGGCA GGAGAATAAC TTGAACCCGG GAGGTGTGGG TTGCAGTGAA 120
CCGAGATCAT GCCACTGCAC TCCAGCCTGG GCGACAGAGT GAGACTTTGT GTCAAAAACA 180
ATAATAATAA TAATAATAAT GCACTAGGTG CAGATACTGA TAAAGGCTTT GTGAGGAATT 240
TTCTTTCTTT CTTTTTTCTT TTTTTTTTGA GACAGAGTCT CACTCTCTTT CCTGGCTGGA 300
GTGCAGTGGC ACGATCTCGG CTCACTGCAA CCTCCGCCTC CCGGGTTCAA GCGATTCTCC 360
TGCCTCAGGC TCCCAAGTGG CTGGGATAAC AGGTGCCCAC CACTACGCCC AGCTAATTTT 420
TTTTTTTTTT TTAGATAGGG TCTGGCTCTG GCTCTGTCAT ACAGGCTGGA GCACAGTGGC 480
ATGATGACAA CCCACTGCAG CCTTGACCTC CTGGGCTTAA GTGATCCTCT TGCCTCAGCC 540
TCCTGAGTAG CTGGGGCTAC AGGCTTATTT TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC 600
CCAGGCTGGT CTCAAACTTC TGGGCTCAAG CAATCCTCCT GCCTTGGCTT CCCAAAGTGC 660
TGGGTTTACA GGAGTGAGCC ACCATGTCTG GCCATTTGAG GAAATTTTTA TTTTTGTCTG 720
TCTTGTTTCC TGCTCTGTCC CCAGCACCTA GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG 780
TGTGTGTGTG TGTGTGTGTG TGTGTAGGTG TGCTGATTAA ATATTTGAAT GGCTGATTGA 840
ATGAACGAAT GAATGTCATC CTACAACCAC TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG 900
GCTGGGGCCC TGGCCTCTGG GATCCCTCTT GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC 960
AGCTCTGTGC TGAAGAGGGC GTGGAGGGGG CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG 1020
GCTGCCTGCC CTGGACAGCA GCCCAGAGTG TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC 1080
CTGAGTCACC CTGGGAGAAA CCCCAGCCAC ATACCTGGCC GCTGACATCA CCCGGCCAGG 1140
GCACCCCCGG CAGCCTAGAC AAGCTGACTG AATCACAGGC GGAATTCAGC CACCCCGGGC 1200
ACGTGGCCTG CTGTGACCCC CCGCAACACC CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG 1260
GCCGGGCACA CAGGGGTCAG TGAGGGGGCA TGGGGCCTGA GTCAGGGACA GGGTGGCTAC 1320
AGCCAGAGAC CACCCAGCCA CAGGCGTCCA TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG 1380
GAGAGCCTGT GGGGAGGCCC TGGCGGGTGA GGAGGAAGCA CGTGTGGGTG TGACGGGGAG 1440
GCTGCGGCTT GTGGGCAGCG GCTGGGCGAC CCACAGGGGT GGGATGGGGT CTGAGTGTTT 1500
GCGCAGAGAA TCACCAAATC GTAAGAGACT TGGTCGTAAG AGTCAGTCAG GAGGACAATG 1560
GAATCACCAA TGTGCTTACA CACGCAAAGG CACACACGCA CACTCAACAC CCGGCCTGGG 1620
GAGGCCCTGA CTCCACCCAC CCCAGGCCAG CGGGGCCTCA CTACCCATAA GCCTGCAAGT 1680
TCCCTAAGGG ACTGAGGCCT AAGGGACAGT TTCCTCATCT GTTGAGTGGG GGTATTAACA 1740
AGCATTATTA GGCCAGGCAC AGTGACTCGT GAGGCAGAGG TAGGCGGATC CCTTGGAGGC 1800
CAGAAGTTCA AGACCAGCCT GGACATCATA GCAAGACCCC TTCTCTACAA AGAAAAAATT 1860
TAAAAATTAG CTGGATGTGG TGGTGTGCAC CTGTAGTCCC AGGTACTCAG GAGGCTGTGG 1920
AGGGTGGATT GCTGGAGTGT TGGAGTTTGA GACTGCAGTG AGCTATTGAT TGCACCACTG 1980
TACTCCAGCC TAGACAACAG AACAAGATCC TATAGCAAAA AAAAAAAAAA AAAAAAATCA 2040
CTATTATTGT AATAGCTATG CTTACGGGGA ACATACTTTC TGCCAGGTGC TGTTCTAGGC 2100
ATTCTACATT TTTTTTTTTT AAATAATGGA GATGACGTCT CACTATGTTT CCCAGGCTGG 2160
TCTTGAACTC CTGAGCTCAG GCTATCCTCT CGCTTTTTTG GTGGCTGGCA CGCCTGTAAT 2220
CCCGACATTT TGGGAGGCCA AGGTGGGTGG ATCGCCGGAG CCCAAGAGTT CGAGACCAGC 2280
CTGGGAAACA TAGTGAGATG CCATCTCTAC CAAAAAATCA AAAAATTAGC TAAGCATGGT 2340
GGCTCATGCC TGTAGTCCCA GCTACTCAGG ATGCTGAGGT GGGAGGATCA CTTGAACCTG 2400
GGAGATGGAA GTTGCAGTAA GCTGAGATTG TGCCACTGCA CTCCAGCCTG GGTGACAGAA 2460
TAAGACCTTG 2470