EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-28746 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr5:180225920-180228260 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs655601chr5180226673hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr5:180227113-180227124GGTGACTCATT+6.02
FOSL2MA0478.1chr5:180227112-180227123GGGTGACTCAT+6.14
JUNMA0488.1chr5:180227873-180227886CTAATGATGTCAT+6.05
JUNBMA0490.1chr5:180227112-180227123GGGTGACTCAT+6.32
POU4F2MA0683.1chr5:180227280-180227296CTGCATAATAAATTAC+6.75
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_00208chr5:180226338-180232837Adipose_Nuclei
SE_04432chr5:180227786-180229455Brain_Anterior_Caudate
SE_09403chr5:180224222-180239890CD14
SE_11617chr5:180223963-180241038CD20
SE_13619chr5:180226362-180227355CD34_Primary_RO01536
SE_14652chr5:180226061-180232679CD4_Memory_Primary_7pool
SE_17640chr5:180224285-180240076CD4p_CD25-_CD45RAp_Naive
SE_18207chr5:180224315-180232594CD4p_CD25-_CD45ROp_Memory
SE_18943chr5:180224402-180232678CD4p_CD25-_Il17-_PMAstim_Th
SE_19487chr5:180224404-180232635CD4p_CD25-_Il17p_PMAstim_Th17
SE_20552chr5:180226045-180232629CD56
SE_21228chr5:180226799-180232526CD8_Memory_7pool
SE_23037chr5:180225369-180239518CD8_primiary
SE_25888chr5:180226182-180232829Duodenum_Smooth_Muscle
SE_26659chr5:180226632-180228299Esophagus
SE_28199chr5:180225732-180231148Fetal_Intestine
SE_29359chr5:180225635-180232008Fetal_Intestine_Large
SE_31515chr5:180227197-180228261Gastric
SE_37805chr5:180225251-180231922HSMMtube
SE_40819chr5:180226144-180232486Left_Ventricle
SE_42229chr5:180225896-180228353Lung
SE_50139chr5:180226026-180232582Sigmoid_Colon
SE_51462chr5:180227840-180239845Skeletal_Muscle
SE_52103chr5:180226153-180230967Skeletal_Muscle_Myoblast
SE_52459chr5:180226161-180232564Small_Intestine
SE_62365chr5:180226988-180260779Tonsil
SE_63877chr5:180226077-180231374HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5180226966180227821
chr5180227892180227963
Enhancer Sequence
AAGTTACTCA TTGACTGCTA GCATCCCATG TCAAGCCCTC CAGCCCTTTA ACCTGAACTC 60
ATTCCTTCGT AGGAAACACT GTTTTAAGTC TGGACTCTTG ATGTAGTTTC CCAGCTGGTC 120
CACCTGTCAC TAATCTTGCT TCCCTCTCAC AAACCTTCCC AACAGCAACA GCGCATCCTT 180
CCTGACAAGT ACACCTGGTC ACGACATTAA CTTGCTTTAA AAACCATCAG AGGCTGCACT 240
GCCCACAAAC TCAAACTCAA ACTCATTATG ATGACATCCA AAGCCCTTCA GACAGACTGT 300
CTGAAACATC CCTTTTCAAC CTTACCTCCA ACCACTAACC CCATGGACCC TGCACTCTGG 360
CCTCAGCAGG CTGCTTTTTC CCCAGTAAGC ATATACCTGG ACGCTGCTGT GTCTCTGCTC 420
CAGCTGGTCC CTCATCCTGG AATTTGACCC ACAGCGCCAC CTGCCAGCCA CCCACACATC 480
CTTTCAGGCC ACTTCAGGTG ACTCCTTCTG TAACATCACA GACAGAGCCA GGCCTCCCTA 540
TGACTACACT CCCACAGCAC TCTCTCCACG CTGTAACAGA ATCTGTGGCC ACGCTGACCT 600
GACTCCCACC TTCCTCCTTA GGAAAAAAGA CTCTATGACC TCTGTGCCCA CCACAGTGCT 660
TGGCACATGT ATGAGGTTCA AGTGGCTGGA TGGAAGACTG CTTGCACTAT TACCGAAATC 720
AGGGAGAAAG ATGGCCAACG CAGCAGCAAG AGAGTGAAGT GTGACATTTT CCAGAGATGA 780
CCGCACATAT CCCATTCCAT ATGCTCTTCT TACAAGTGAT AAAGACACTC CTGCCTCCAG 840
AGCTGAGGGT CTATGTTCCC TCCCTTTGGT TCTGGGAAGA GATGCTATGT GACTTGTGAG 900
ACTAACTCAT AAAAGGCAGT AGTTTCCACC TGGTCCTCTT AAGATGCTGA CTCCTAGGAC 960
CCTGCTATAT GGACAGGACA CTGCTACATG GACAGGACCC CCATAGGTAT TCCAACTGAC 1020
CACCCCAGCT AAGGTCCCAG CTGACAGCCA GCATCAACCG CTAGACACAG GAGACAGCCC 1080
TCCAGATTAT CCCAGCCCCA GCTGACTGCA ATGGCGTGAA AGACCACAAG CAAGAACCAC 1140
ATAGCTGAGA TGTTAATAAA ATGATTCTGT TGTTGTAAGC CACTAAGTTC TGGGGTGACT 1200
CATTATGCAG CCATCAGTAC CTGAAGCAAT GAGAGAAACA GACTCTAGAT AATCTTGACA 1260
AGCAGGGCAA GTGCCCTCCC TGCCCTCTGT GCTCAGCTCC AAGTCCAAAC ACTGAGGCCC 1320
TGTCTCCACT CATGTCTCCT TCCTTAGTAG GTATCTACTC CTGCATAATA AATTACCTCG 1380
ATATTTAGTG GCTTAAAACA ATAGTTATCA CTTACTCCTC ACAGTTTCTA TTGGTCAGAA 1440
ATGTGGACAG TGCAGCACAG AGGAGATGAC GTGTCTCTGC TCCACTATGC CTGAGGCCTT 1500
GCTGAAAGAC TCAAAAGCTG AGGGCCAGAT GCCCCTAGAG GCTCTCACAT TCTCTCACAT 1560
GTCTGTAGGA TGATGTTGGC AGCAGCTGAG ACCTTATCAG CAGGAGTGCT CACTAGAACC 1620
CCTCTATGTG GCCTGGAAAT GTCCTGGAAG TGGTGGCTGC ATTCCAAAGG TGAGTGTTCC 1680
AAGAAAGCGG GCAAGCCAGG TGAAAGTGTA TCCTGTTCCT GATTCAGCCT TGGATCAGGT 1740
CTGTCTTACT CACTGGTCAA GGGAACCACA AGTCCCTATT GACATGCAAG GGGAGAGAAT 1800
CATAAACCCC ACCACTAGGT GGGAAGTGGA CAATGTCAAA CTATAACTAC ATGTGGAAGG 1860
GGATACTTAC GGGTGAGGCC CTTGAGGGAA AATACAATCT GCTACACCTT CCTTTTTAAA 1920
TAGAACAACT GCCCTTAATC CTGACCTGAG TTCCTAATGA TGTCATTTAT GAGACTGGCA 1980
TGCAAGGCAC AGACTCAAAA CTGGCTTTGA CTTTCTAGAG TTTTCACAAC TCCTTTAGGG 2040
AGGTGACACA GCCAATCCAC ACCACCAGGT ACAAAGACAT CTGCACCATG GTGGGAGATG 2100
AGAAGTGAGT CTTTTCAGTA CAAAACCCTT CAGCTAAAAC CGAGGTGGCT CTGGGTAGGC 2160
GCCACCTGCC CCTATGGGGC TCACTCAGTT TCTGAAGCAT TTGAAGGACT GCCTAGGAGC 2220
TGTGAGATCC TTTCTAACAC TCTGATACCA TGGTGTTCTC CAGCCTATTT CCTTTATCTG 2280
GCAAAAAATG TTTCTTAAAT AGCAAGTGAA CACCAGATAG TCAACTTCCA ATCATGAGCA 2340