EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-27437 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr5:131812540-131814940 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs13164856chr5131813204hg19
rs7719499chr5131814091hg19
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
PLAG1MA0163.1chr5:131813583-131813597CCCCCTGGGGCCCC-6.65
RESTMA0138.2chr5:131813317-131813338GCATCTGTGCATGGTCCTGAG-6.64
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00037chr5:131812560-131817272Adipose_Nuclei
SE_09163chr5:131813711-131816157CD14
SE_10340chr5:131812465-131814665CD19_Primary
SE_10915chr5:131798063-131818030CD20
SE_11856chr5:131812476-131813459CD3
SE_11856chr5:131813642-131816146CD3
SE_13479chr5:131813131-131813828CD34_Primary_RO01536
SE_14495chr5:131813953-131815483CD4_Memory_Primary_7pool
SE_16304chr5:131814540-131816315CD4_Naive_Primary_8pool
SE_17370chr5:131811673-131815833CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131804786-131818044CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131813692-131817848CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131813767-131816162CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131797758-131816289CD56
SE_22284chr5:131797996-131818026CD8_primiary
SE_23079chr5:131810420-131815180Colon_Crypt_1
SE_23750chr5:131812423-131812831Colon_Crypt_2
SE_23750chr5:131812907-131814847Colon_Crypt_2
SE_25340chr5:131808656-131817904DND41
SE_25784chr5:131810212-131813275Duodenum_Smooth_Muscle
SE_25784chr5:131813486-131815448Duodenum_Smooth_Muscle
SE_26597chr5:131812711-131813914Esophagus
SE_27629chr5:131808629-131817861Fetal_Intestine
SE_28559chr5:131808476-131817875Fetal_Intestine_Large
SE_30917chr5:131812828-131815508Fetal_Thymus
SE_31393chr5:131812920-131814268Gastric
SE_39368chr5:131812547-131813127Jurkat
SE_39368chr5:131813131-131815907Jurkat
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_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131811691-131812788Pancreatic_islets
SE_66244chr5:131812547-131813127Jurkat
SE_66244chr5:131813131-131815907Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr5131813702131813794
chr5131813166131814588
chr5131812683131813109
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
TCTCCCCATC CCAACAAGCC AAGCAGGAGC ACTTGGAGGG GAGCCCTGGG TCCCCAGCAG 60
AAACAGCCCT CCACTGCCTC CACAATCAGG TCATCAGCCC CTGCCCCAGT CCACTGTTGC 120
CCTAGTGTGG CCGACATGAC AGGACTTCTT GTAATTCTGG CCTAATGGTT CCCACATCCC 180
CAAACACCAA CTCCATGTCC ATATGCCTCC CTTGTTACAC AAAGTCAGCT TTCTCCAAGA 240
AACCAGAGAA GCACATGATC CCCGCCACAC CTCTCCAGGG GCCTCCCTCC TGATCTGAGA 300
TCCTCGGTAT ATCCCATGGC CTCTCTGAGC CAAGGTGTAG CTGAGTTGTG TGGGGTTTTT 360
GTTTGTTTGT TTGTTTAACC ACTGTGTAAG AACTCACTAC TTGGGCCCCA ATTCTGGACA 420
AATTCCAGAT TGACAGTGTG AGGGAGAGGT GGTAGCAGAA CTGGACACCC CCACAACCTT 480
GTTGCTTTGA AGGAAAGAAG GAGGGCAGAA ACAGGAGGGG ATCCAGCCAA TCCAAGGCAT 540
TTGGCCCGAA ATGGATGTGA AGACCTCACC CAGGCTGCCC CTCTGGGCTG GCACAGGAGG 600
GCAGGGGAGG GCCTTCCCTA AAGGAAGCCT GCAGGTGAAT CCCAGCGCCC GCCTGATGTA 660
AGGTGGCAAC TGGCCAGCAG CCAGAGGTGC CAGGTGTTCT CAGGGATCAA GAAACCAGGA 720
ATTAGGCCCA CCAGAGCCAT AGGGTCTGAC CCGAGCCTGG TGGCTGGGAA TGAGAATGCA 780
TCTGTGCATG GTCCTGAGTC TCACAGCCAT CCAGGGTCCA GACCTCTGAG GAACTCCAGG 840
ACCCAACAGA GGGTCTGGTT TAAAGCAGAA CAGGAGACTA GGTTGTCTTG CTGAGACAGA 900
AACATGGCTA AAAAGTCCTC TTTGATCCTG GGAGCTGAGA TAAGGCCTAG CAGGCCAGAG 960
TCCCCCGTTT GCTCCAAACA GGCCTGGTGT GGCCAAGCTG CCCCCTGCAC TGAGGCCAAG 1020
TTACAAGCCT GTCTGTGTCT CGGCCCCCTG GGGCCCCACC CTTCGAAACT GCAGGTGGCC 1080
TCCAGGGCAT AGGTGGGGCA AACCCTACCC TGTTGGGGCC CTGGGGCCTG TAGCGGCAGA 1140
GCCATGTTGC CAGGGGTGTT GGAAGGTGTG TGTGCTGGGG GAAGGGAGGA GAGCTGAAGG 1200
CAGGGCAGCA CAGCAGCTGC AGCTTTTGCC GCCTTCCCTC AGCATCCACA AGTGCTTGCT 1260
TGGCATAAGG TGCTCGGGCC CTGCCCCTTG CTAGCTCTCC CCAGCTTCTT GTGCAGGCCT 1320
CCGTGTTCTT CTCTCAGGCA GCCTGATATG GAACCAACCT GGATTCTGGG CACAGATAGA 1380
TGATGTGGGT TGGAACCAAG GCTCCATACT GATTAGGTGG TGAGAGTTGG TTTCCTGGTC 1440
TGTGAACAAG GGCCGTGGTG GGGTGCCAGT GCCGTGGTAC ACACGTGGTG CTTGGCATAG 1500
CACCCAGCAC AAAGTGAGCA CTCGAGGCCT GTGTTGCCAT TATCCAGCCA CACTTTGAGG 1560
TCTTTTCCAG TTCTGCTCAT TTGTGAGCTT GTGGGATCAT CTCCTTGGGT GAGGAATGGT 1620
GGGCTGGACG TCTGCCTCCC CTCTTTCATT CAGTCCCCAT GTCCTTGCTC CATAGCCTCC 1680
AGTATCTCCC CAGCTGAAGT TTCACTCAGC AGACTCTGCA GGCTTGTGTC TTACCACTGA 1740
GCCAGCAGAG GTGGACTTCT GTAACTCCTT ACCCTGAGAA AACCAGCATA AATGGGTCTC 1800
TTGAGAGCTG CCTGGAGCTA GGAAAACTAT GCGGCCAGCC AGCTATACCC TTCTGAGGCC 1860
TTAGACTTGG CCCCACAAGG GAGCTCCGGA TGATAAAGCC AAGCTCCACC CTGCCAAGTA 1920
CTTTCACCCC TGGAAAAGGA GGGCACCAGC TTCCCCTTCT CCCACCCCAG GCCTCCTTCC 1980
TCTGTGACAG CCAGCAGAAC TGGGGAAAGG TTAGTGCTGA GTTCTGATGA ATTGGAAGAT 2040
CAGTTGTGCC CAAGTTAAGG AACAGCATTA CATCTGACAG AGACAAAAGC TTTCTATAGG 2100
GTCACTATAT TAGCCCTGGG TGCTCCAACA GGACTGCCTG GAGGACATCT GTACCCCCTT 2160
TCCCCTCCAA GTATAAGGGC AGAGTTTTGG ATCTGTACAC AGTGTGAAAG ATCAAGTGGT 2220
CCCAGAGAAT GACAACCTGG CTGTTTCCCA GCCCCACCAA CCAGGAGACA TCACTCCTAG 2280
AGAAAAAAAC TCCACTTCCC AGGGCTACCC CAGGATTTCA GTTCCCACTT TGGCAGGCCC 2340
CACTGGAGAC TTCCAGAAAA ATCAGAGAAA GCTCTTTCCT TTGGAGTTGT AATGGTCACA 2400