EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-40602 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr19:45958450-45960280 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr19:45959150-45959161CTGAGTCACCC-6.02
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
CTGGGATAAC AGGTGCCCAC CACTACGCCC AGCTAATTTT TTTTTTTTTT TTAGATAGGG 60
TCTGGCTCTG GCTCTGTCAT ACAGGCTGGA GCACAGTGGC ATGATGACAA CCCACTGCAG 120
CCTTGACCTC CTGGGCTTAA GTGATCCTCT TGCCTCAGCC TCCTGAGTAG CTGGGGCTAC 180
AGGCTTATTT TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT CTCAAACTTC 240
TGGGCTCAAG CAATCCTCCT GCCTTGGCTT CCCAAAGTGC TGGGTTTACA GGAGTGAGCC 300
ACCATGTCTG GCCATTTGAG GAAATTTTTA TTTTTGTCTG TCTTGTTTCC TGCTCTGTCC 360
CCAGCACCTA GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 420
TGTGTAGGTG TGCTGATTAA ATATTTGAAT GGCTGATTGA ATGAACGAAT GAATGTCATC 480
CTACAACCAC TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC TGGCCTCTGG 540
GATCCCTCTT GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC TGAAGAGGGC 600
GTGGAGGGGG CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC CTGGACAGCA 660
GCCCAGAGTG TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC CTGAGTCACC CTGGGAGAAA 720
CCCCAGCCAC ATACCTGGCC GCTGACATCA CCCGGCCAGG GCACCCCCGG CAGCCTAGAC 780
AAGCTGACTG AATCACAGGC GGAATTCAGC CACCCCGGGC ACGTGGCCTG CTGTGACCCC 840
CCGCAACACC CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG GCCGGGCACA CAGGGGTCAG 900
TGAGGGGGCA TGGGGCCTGA GTCAGGGACA GGGTGGCTAC AGCCAGAGAC CACCCAGCCA 960
CAGGCGTCCA TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT GGGGAGGCCC 1020
TGGCGGGTGA GGAGGAAGCA CGTGTGGGTG TGACGGGGAG GCTGCGGCTT GTGGGCAGCG 1080
GCTGGGCGAC CCACAGGGGT GGGATGGGGT CTGAGTGTTT GCGCAGAGAA TCACCAAATC 1140
GTAAGAGACT TGGTCGTAAG AGTCAGTCAG GAGGACAATG GAATCACCAA TGTGCTTACA 1200
CACGCAAAGG CACACACGCA CACTCAACAC CCGGCCTGGG GAGGCCCTGA CTCCACCCAC 1260
CCCAGGCCAG CGGGGCCTCA CTACCCATAA GCCTGCAAGT TCCCTAAGGG ACTGAGGCCT 1320
AAGGGACAGT TTCCTCATCT GTTGAGTGGG GGTATTAACA AGCATTATTA GGCCAGGCAC 1380
AGTGACTCGT GAGGCAGAGG TAGGCGGATC CCTTGGAGGC CAGAAGTTCA AGACCAGCCT 1440
GGACATCATA GCAAGACCCC TTCTCTACAA AGAAAAAATT TAAAAATTAG CTGGATGTGG 1500
TGGTGTGCAC CTGTAGTCCC AGGTACTCAG GAGGCTGTGG AGGGTGGATT GCTGGAGTGT 1560
TGGAGTTTGA GACTGCAGTG AGCTATTGAT TGCACCACTG TACTCCAGCC TAGACAACAG 1620
AACAAGATCC TATAGCAAAA AAAAAAAAAA AAAAAAATCA CTATTATTGT AATAGCTATG 1680
CTTACGGGGA ACATACTTTC TGCCAGGTGC TGTTCTAGGC ATTCTACATT TTTTTTTTTT 1740
AAATAATGGA GATGACGTCT CACTATGTTT CCCAGGCTGG TCTTGAACTC CTGAGCTCAG 1800
GCTATCCTCT CGCTTTTTTG GTGGCTGGCA 1830