EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS023-13299 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr19:45958320-45960530 
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
CTTTTTTCTT TTTTTTTTGA GACAGAGTCT CACTCTCTTT CCTGGCTGGA GTGCAGTGGC 60
ACGATCTCGG CTCACTGCAA CCTCCGCCTC CCGGGTTCAA GCGATTCTCC TGCCTCAGGC 120
TCCCAAGTGG CTGGGATAAC AGGTGCCCAC CACTACGCCC AGCTAATTTT TTTTTTTTTT 180
TTAGATAGGG TCTGGCTCTG GCTCTGTCAT ACAGGCTGGA GCACAGTGGC ATGATGACAA 240
CCCACTGCAG CCTTGACCTC CTGGGCTTAA GTGATCCTCT TGCCTCAGCC TCCTGAGTAG 300
CTGGGGCTAC AGGCTTATTT TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT 360
CTCAAACTTC TGGGCTCAAG CAATCCTCCT GCCTTGGCTT CCCAAAGTGC TGGGTTTACA 420
GGAGTGAGCC ACCATGTCTG GCCATTTGAG GAAATTTTTA TTTTTGTCTG TCTTGTTTCC 480
TGCTCTGTCC CCAGCACCTA GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG 540
TGTGTGTGTG TGTGTAGGTG TGCTGATTAA ATATTTGAAT GGCTGATTGA ATGAACGAAT 600
GAATGTCATC CTACAACCAC TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC 660
TGGCCTCTGG GATCCCTCTT GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC 720
TGAAGAGGGC GTGGAGGGGG CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC 780
CTGGACAGCA GCCCAGAGTG TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC CTGAGTCACC 840
CTGGGAGAAA CCCCAGCCAC ATACCTGGCC GCTGACATCA CCCGGCCAGG GCACCCCCGG 900
CAGCCTAGAC AAGCTGACTG AATCACAGGC GGAATTCAGC CACCCCGGGC ACGTGGCCTG 960
CTGTGACCCC CCGCAACACC CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG GCCGGGCACA 1020
CAGGGGTCAG TGAGGGGGCA TGGGGCCTGA GTCAGGGACA GGGTGGCTAC AGCCAGAGAC 1080
CACCCAGCCA CAGGCGTCCA TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT 1140
GGGGAGGCCC TGGCGGGTGA GGAGGAAGCA CGTGTGGGTG TGACGGGGAG GCTGCGGCTT 1200
GTGGGCAGCG GCTGGGCGAC CCACAGGGGT GGGATGGGGT CTGAGTGTTT GCGCAGAGAA 1260
TCACCAAATC GTAAGAGACT TGGTCGTAAG AGTCAGTCAG GAGGACAATG GAATCACCAA 1320
TGTGCTTACA CACGCAAAGG CACACACGCA CACTCAACAC CCGGCCTGGG GAGGCCCTGA 1380
CTCCACCCAC CCCAGGCCAG CGGGGCCTCA CTACCCATAA GCCTGCAAGT TCCCTAAGGG 1440
ACTGAGGCCT AAGGGACAGT TTCCTCATCT GTTGAGTGGG GGTATTAACA AGCATTATTA 1500
GGCCAGGCAC AGTGACTCGT GAGGCAGAGG TAGGCGGATC CCTTGGAGGC CAGAAGTTCA 1560
AGACCAGCCT GGACATCATA GCAAGACCCC TTCTCTACAA AGAAAAAATT TAAAAATTAG 1620
CTGGATGTGG TGGTGTGCAC CTGTAGTCCC AGGTACTCAG GAGGCTGTGG AGGGTGGATT 1680
GCTGGAGTGT TGGAGTTTGA GACTGCAGTG AGCTATTGAT TGCACCACTG TACTCCAGCC 1740
TAGACAACAG AACAAGATCC TATAGCAAAA AAAAAAAAAA AAAAAAATCA CTATTATTGT 1800
AATAGCTATG CTTACGGGGA ACATACTTTC TGCCAGGTGC TGTTCTAGGC ATTCTACATT 1860
TTTTTTTTTT AAATAATGGA GATGACGTCT CACTATGTTT CCCAGGCTGG TCTTGAACTC 1920
CTGAGCTCAG GCTATCCTCT CGCTTTTTTG GTGGCTGGCA CGCCTGTAAT CCCGACATTT 1980
TGGGAGGCCA AGGTGGGTGG ATCGCCGGAG CCCAAGAGTT CGAGACCAGC CTGGGAAACA 2040
TAGTGAGATG CCATCTCTAC CAAAAAATCA AAAAATTAGC TAAGCATGGT GGCTCATGCC 2100
TGTAGTCCCA GCTACTCAGG ATGCTGAGGT GGGAGGATCA CTTGAACCTG GGAGATGGAA 2160
GTTGCAGTAA GCTGAGATTG TGCCACTGCA CTCCAGCCTG GGTGACAGAA 2210