EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS118-15342 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr5:131811740-131813220 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs13164856chr5131813204hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr5:131813031-131813049GGAAAGAAGGAGGGCAGA+6.17
EWSR1-FLI1MA0149.1chr5:131813027-131813045TGAAGGAAAGAAGGAGGG+6.63
Foxd3MA0041.1chr5:131812900-131812912GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr5:131812904-131812916GTTTGTTTGTTT+6.32
Hnf4aMA0114.3chr5:131811810-131811826TGGGGACTTTGACCTT-6
RREB1MA0073.1chr5:131812442-131812462CCCCACCCCACCCCTACCCC+6.68
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00037chr5:131810090-131812540Adipose_Nuclei
SE_00037chr5:131812560-131817272Adipose_Nuclei
SE_01257chr5:131811740-131812431Adrenal_Gland
SE_06435chr5:131810039-131812439Brain_Hippocampus_Middle
SE_10340chr5:131812465-131814665CD19_Primary
SE_10915chr5:131798063-131818030CD20
SE_11856chr5:131812476-131813459CD3
SE_17370chr5:131811673-131815833CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131804786-131818044CD4p_CD25-_CD45ROp_Memory
SE_19972chr5:131797758-131816289CD56
SE_22284chr5:131797996-131818026CD8_primiary
SE_23079chr5:131810420-131815180Colon_Crypt_1
SE_23750chr5:131811731-131812301Colon_Crypt_2
SE_23750chr5:131812423-131812831Colon_Crypt_2
SE_23750chr5:131812907-131814847Colon_Crypt_2
SE_25340chr5:131808656-131817904DND41
SE_25784chr5:131810212-131813275Duodenum_Smooth_Muscle
SE_26597chr5:131812711-131813914Esophagus
SE_27629chr5:131808629-131817861Fetal_Intestine
SE_28559chr5:131808476-131817875Fetal_Intestine_Large
SE_30917chr5:131812828-131815508Fetal_Thymus
SE_31393chr5:131811636-131812208Gastric
SE_31393chr5:131812920-131814268Gastric
SE_39368chr5:131811792-131812447Jurkat
SE_39368chr5:131812547-131813127Jurkat
SE_40726chr5:131809980-131815612Left_Ventricle
SE_42103chr5:131809951-131815230Lung
SE_48659chr5:131810417-131814893Right_Atrium
SE_50023chr5:131812548-131815406RPMI-8402
SE_50051chr5:131808593-131816260Sigmoid_Colon
SE_52336chr5:131808690-131816220Small_Intestine
SE_53285chr5:131809900-131816337Spleen
SE_54554chr5:131810068-131812535Stomach_Smooth_Muscle
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131811691-131812788Pancreatic_islets
SE_66244chr5:131811792-131812447Jurkat
SE_66244chr5:131812547-131813127Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5131812683131813109
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
TCTATCTCCA GTACTGCCGA AAAGAGACAA GCGGTCATGC TGCATGTCAT GCACACACTG 60
GCCCTTGTTC TGGGGACTTT GACCTTGGCT GCTGGTTGGT CATGGCCTGT TTTGCCCAGG 120
GCTCTACTGC AGGGGCAGGG TTGGTTATTC CTCTGTGCCC TTTTTGCCTC TCAGCCTGCC 180
TGCTCCTCTG GACCCCAGAG TCTAGCCTGG TTCCCCCAGG GGAGGGACTC AGAAAGTGCT 240
ACTATAGAGA GATGCTAACT ACATCTCTGC TGAGCAGCAG GAGATGCTCT GAAGTGCCAA 300
TCCTGGCTGA ACACTGTGAG AATATGGAAG AGATAAGCTG CTTGCCCCTG GGGAGCTTCC 360
AGTCTGGTTG GCGAGATTGG GTACCCCGCA GACCCTGTGG GGACTGGCAG ACAGGAAGGG 420
ACAGGCCCTA GAGGGTGAGG CTTTGCCTGT GAGGGCTGTC ACTGGTCAGA GAAGGGAGGG 480
CCCCAGGGCT CCATTGTACA AGTCTTAGGA TGGCCAAAGA CCAAAAATGG GGTCCTCTTC 540
AGTGACCTGA GGCAGGCCGC ACAAGCTTGG GGGTAGATGG TCTCCTGTGC CCAGAACTCT 600
GGCTGCTCGC CACCTATGAC AGAAGAATGG TGATGAACAC TCACCAGGCT GTTCCAAGTC 660
TCGGAAAGTT GGACACCCCT TCAGGTCCTC CTCCCTGTCC CACCCCACCC CACCCCTACC 720
CCATATGGGA ATGCCAGGCT GTAGCCTTCG CTGTGACCCA TCCCAACTCC AGCTCCTCTC 780
CCCATCCCAA CTCCAGCTCC TCTCCCCATC CCAACAAGCC AAGCAGGAGC ACTTGGAGGG 840
GAGCCCTGGG TCCCCAGCAG AAACAGCCCT CCACTGCCTC CACAATCAGG TCATCAGCCC 900
CTGCCCCAGT CCACTGTTGC CCTAGTGTGG CCGACATGAC AGGACTTCTT GTAATTCTGG 960
CCTAATGGTT CCCACATCCC CAAACACCAA CTCCATGTCC ATATGCCTCC CTTGTTACAC 1020
AAAGTCAGCT TTCTCCAAGA AACCAGAGAA GCACATGATC CCCGCCACAC CTCTCCAGGG 1080
GCCTCCCTCC TGATCTGAGA TCCTCGGTAT ATCCCATGGC CTCTCTGAGC CAAGGTGTAG 1140
CTGAGTTGTG TGGGGTTTTT GTTTGTTTGT TTGTTTAACC ACTGTGTAAG AACTCACTAC 1200
TTGGGCCCCA ATTCTGGACA AATTCCAGAT TGACAGTGTG AGGGAGAGGT GGTAGCAGAA 1260
CTGGACACCC CCACAACCTT GTTGCTTTGA AGGAAAGAAG GAGGGCAGAA ACAGGAGGGG 1320
ATCCAGCCAA TCCAAGGCAT TTGGCCCGAA ATGGATGTGA AGACCTCACC CAGGCTGCCC 1380
CTCTGGGCTG GCACAGGAGG GCAGGGGAGG GCCTTCCCTA AAGGAAGCCT GCAGGTGAAT 1440
CCCAGCGCCC GCCTGATGTA AGGTGGCAAC TGGCCAGCAG 1480