EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS118-15338 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr5:131757830-131759990 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr5:131757926-131757938GTTTGTTTGTTT+6.32
Nr2f6(var.2)MA0728.1chr5:131758148-131758163TGAACTCCTGACCTC-6.22
RARA(var.2)MA0730.1chr5:131759855-131759872TCACCCTTGCTTGACCT-6.72
SP2MA0516.2chr5:131758438-131758455TGGTGGGTGGGGCTTAG-7.1
Number of super-enhancer constituents: 49             
IDCoordinateTissue/cell
SE_00037chr5:131744052-131766081Adipose_Nuclei
SE_01257chr5:131758434-131759589Adrenal_Gland
SE_02141chr5:131758298-131759686Aorta
SE_04124chr5:131758326-131759535Brain_Anterior_Caudate
SE_09163chr5:131754698-131768049CD14
SE_10413chr5:131754780-131764629CD19_Primary
SE_10915chr5:131741116-131769232CD20
SE_11905chr5:131758194-131759326CD3
SE_11905chr5:131759437-131767697CD3
SE_13055chr5:131758245-131759557CD34_Primary_RO01480
SE_13453chr5:131754417-131768040CD34_Primary_RO01536
SE_14162chr5:131757793-131764759CD34_Primary_RO01549
SE_14574chr5:131754589-131769241CD4_Memory_Primary_7pool
SE_17470chr5:131754338-131768227CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131754003-131768718CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131754349-131769426CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131758066-131768041CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131754313-131769496CD56
SE_20885chr5:131754675-131766460CD8_Memory_7pool
SE_22150chr5:131758139-131759843CD8_Naive_8pool
SE_22284chr5:131754357-131780344CD8_primiary
SE_23079chr5:131757777-131765509Colon_Crypt_1
SE_23750chr5:131758176-131759968Colon_Crypt_2
SE_25340chr5:131744602-131768034DND41
SE_25784chr5:131758078-131768069Duodenum_Smooth_Muscle
SE_26597chr5:131758001-131760112Esophagus
SE_27859chr5:131757729-131766672Fetal_Intestine
SE_28909chr5:131757525-131766711Fetal_Intestine_Large
SE_30917chr5:131758162-131767980Fetal_Thymus
SE_31393chr5:131757800-131765373Gastric
SE_32566chr5:131754945-131764808GM12878
SE_39368chr5:131758209-131767951Jurkat
SE_40726chr5:131757690-131766735Left_Ventricle
SE_42103chr5:131757720-131766796Lung
SE_43553chr5:131754361-131767961MM1S
SE_45155chr5:131757995-131759546NHLF
SE_46095chr5:131757999-131759916Osteoblasts
SE_48659chr5:131757913-131759690Right_Atrium
SE_50034chr5:131757766-131768037RPMI-8402
SE_50051chr5:131757730-131767792Sigmoid_Colon
SE_52336chr5:131757743-131768421Small_Intestine
SE_53285chr5:131757733-131765501Spleen
SE_54554chr5:131758856-131766307Stomach_Smooth_Muscle
SE_59850chr5:131745223-131774088Ly4
SE_61542chr5:131744876-131774119Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131758592-131759889Pancreatic_islets
SE_66244chr5:131758209-131767951Jurkat
SE_67252chr5:131754361-131767961MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5131758048131759382
chr5131758280131759109
Number: 1             
IDChromosomeStartEnd
GH05I132418chr5131754337131769271
Enhancer Sequence
AAAAAAAAGA ATAGGAAGCA CGGTTGGCCC TCCATACCAG CAGGTTCTGT GTGTGGACCT 60
GTGGATACGG AGGGCTGACT GTGCTACACA TTTTTTGTTT GTTTGTTTTT TGTTTTTGAG 120
ATGAAGTCTC ACTCTGTCAC CCAGGCTGGA GTGCAGTGGT GCGATCTTGG CTTATTGCAA 180
CCTCCGCCTC CCGGATCCAT GCAATTCTCA TGCCTCAGCC TCCCGAGTGG CTGGGACTAC 240
AAGTGCATGC CACCAAGCCC GCCTATTTTT TGTATTTTTA GAGGAGACGG GGTTTCACCA 300
TGTTGGCGAG GCTGGTCTTG AACTCCTGAC CTCAAGTGAG CTGCCCACCT CGGTCTCCCA 360
AAGTGCTGGG ATTACAGGCA CGAGCCATTG TACCCAGCCC TACGTCACTT TTTATAAGGA 420
ATTTGAGCAT CGTGGCTTTT GGTATCTGAG GAGCTGTCCT GGAACCAATT CCTCGAAGAT 480
GCTAAGGGAC AACTGTAATA GGCTTCTGAA TGGGGGACAA CTGACTGTTT TAAATAGGAA 540
CTTTTATTTC CATTTTACAT CTGCTTTTCA AATAATGTCT TTTCAAATAA TTCTCCAAGG 600
TCACAGGTTG GTGGGTGGGG CTTAGATCTG CCAGACTCCA GAGTCCATGT ACACGCTAAC 660
CCCTGCACTG GCTTGCATTA TCTCCAGACA CAGGTTGGCC TGCATGTGAC CAAGGCTCCA 720
CCCAGCCCTG ACCTTGGATG ACTCTGAGTC TATACATAGC TGCATTTGCG TGTCAGCCTC 780
ACTCCCTGGG CTGAACTGTT TATAGGGTGA AAGGGGACTT TGGGTAAGTC ACTTCCCTGT 840
CTTTCTGAGA CTCTAGGAAA TCAGGGGCAG GAACTCAGCT ATGCATCCAT GGTCTGCACA 900
GCAGCAGCCC AGATAAGTTC CAAGAGCTGC AGAGGCTGTC AGAGAAGCTT CAGAGCTGTA 960
GGTCCCTGGG CAAGTCTCCT CCAAAGTGGG AGCTGCAGGG CTGATGCGGA TCCAGGCAAG 1020
GTGACAGCAC AGCACAAGTT GACTCCTGTT ACTGCCCTAA TCGTCCAGCA TAGGCAGGAG 1080
GAGTTGGGGA TTTGAAGTTT GAAGTTCGAG GAGTTGAACT TTGAAGTTCT TTATGCATTC 1140
CTTTGTCATT CCTTCATAGA ATATTCAGCA AATAACTTAG CACCTAATTG TTCCAGGTCT 1200
GGCCCTGGGC CCTGGGCTTA CAGCAAGGAA CAAAACAACC CAAGTCCCTG CCCTGGTGCC 1260
ACTTACATTC CAGTTGGGGA GACAGACAAT GTATAACACA ATGTTAAGGA GCAGTGAAGT 1320
AGAAGAGGAA AGCAGGGAGA GGGGATAGAG TACTAGGGCC AGAGACCTAG AGGTCCAGGA 1380
AGGCCTCTCT AAGGAGGAGC ATTTGTGCAG AAACCTGGCA TTTGAGCTAG CCAGGGAGCT 1440
AGCAATGTGA ATGTCTAGGT TGCAGGCAGA GGGAATGGCA AGTTCATAGA CCTGAGGTGG 1500
GATTGCCTGG GAAGCAGCGA GTAGGGCAAC GCATTAGGGA GAGAGGAGAG TGGGAAGAGC 1560
CCAGGCTGCA TGGGGCCAGA CCTTGCCACC TTGCCAGCTA TTGAAGAAAG GTAGGGTTTT 1620
GTTCTTTCTC CAGCTCTAAG GTATGTTTCA GGCATCGTTC CTGGCTGACT GGCTCTAAAT 1680
CTGCAGCCCT CCCAGAGAGC CTTTGATCAA CCCAGTATCC TCCTATATCA TCCCTTTTCT 1740
GGCTGAACTA ACCACTGTTC ATTCTGTTGT CTACAACTAT GAACCCTGCC TAATACAGAG 1800
CTTTGGAGGA GGAGGAGAGT GCCAACCAGC TTTATAAGGA AATTAAATAT GTTTTTAAGG 1860
TTGGAAAAGA TGCACTTGGA TATTATACTA AAACGTTTAA ACTTTGGTAG AAAGGGCTCC 1920
ACCTTGGCCA TGCAAAGGGG CCTTTGTCAT CACTGTTTCC TCCCCTAGGA GCCAGGAGGC 1980
TGGGGTCAGT CTCCTCCTTA CCTGCCAGCC AGGGGCCTAA GCTGGTCACC CTTGCTTGAC 2040
CTTCGTGGTC TCACCTGTAT AATTCAGTTA GTTATATTAT TCCTGCCTGA AGGGAAAGAG 2100
GAATGACTTA TTGAGGGTCA TTTCTATGTT GGAGGTCTCT GATGTTGCGA ATAAGTTCCA 2160