EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS110-02468 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr19:45958520-45959910 
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
GCTCTGTCAT ACAGGCTGGA GCACAGTGGC ATGATGACAA CCCACTGCAG CCTTGACCTC 60
CTGGGCTTAA GTGATCCTCT TGCCTCAGCC TCCTGAGTAG CTGGGGCTAC AGGCTTATTT 120
TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT CTCAAACTTC TGGGCTCAAG 180
CAATCCTCCT GCCTTGGCTT CCCAAAGTGC TGGGTTTACA GGAGTGAGCC ACCATGTCTG 240
GCCATTTGAG GAAATTTTTA TTTTTGTCTG TCTTGTTTCC TGCTCTGTCC CCAGCACCTA 300
GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTAGGTG 360
TGCTGATTAA ATATTTGAAT GGCTGATTGA ATGAACGAAT GAATGTCATC CTACAACCAC 420
TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC TGGCCTCTGG GATCCCTCTT 480
GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC TGAAGAGGGC GTGGAGGGGG 540
CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC CTGGACAGCA GCCCAGAGTG 600
TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC CTGAGTCACC CTGGGAGAAA CCCCAGCCAC 660
ATACCTGGCC GCTGACATCA CCCGGCCAGG GCACCCCCGG CAGCCTAGAC AAGCTGACTG 720
AATCACAGGC GGAATTCAGC CACCCCGGGC ACGTGGCCTG CTGTGACCCC CCGCAACACC 780
CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG GCCGGGCACA CAGGGGTCAG TGAGGGGGCA 840
TGGGGCCTGA GTCAGGGACA GGGTGGCTAC AGCCAGAGAC CACCCAGCCA CAGGCGTCCA 900
TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT GGGGAGGCCC TGGCGGGTGA 960
GGAGGAAGCA CGTGTGGGTG TGACGGGGAG GCTGCGGCTT GTGGGCAGCG GCTGGGCGAC 1020
CCACAGGGGT GGGATGGGGT CTGAGTGTTT GCGCAGAGAA TCACCAAATC GTAAGAGACT 1080
TGGTCGTAAG AGTCAGTCAG GAGGACAATG GAATCACCAA TGTGCTTACA CACGCAAAGG 1140
CACACACGCA CACTCAACAC CCGGCCTGGG GAGGCCCTGA CTCCACCCAC CCCAGGCCAG 1200
CGGGGCCTCA CTACCCATAA GCCTGCAAGT TCCCTAAGGG ACTGAGGCCT AAGGGACAGT 1260
TTCCTCATCT GTTGAGTGGG GGTATTAACA AGCATTATTA GGCCAGGCAC AGTGACTCGT 1320
GAGGCAGAGG TAGGCGGATC CCTTGGAGGC CAGAAGTTCA AGACCAGCCT GGACATCATA 1380
GCAAGACCCC 1390