EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS165-12457 
Organism
Homo sapiens 
Tissue/cell
Ramos 
Coordinate
chr5:131813110-131814220 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs13164856chr5131813204hg19
rs7719499chr5131814091hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PLAG1MA0163.1chr5:131813583-131813597CCCCCTGGGGCCCC-6.65
RESTMA0138.2chr5:131813317-131813338GCATCTGTGCATGGTCCTGAG-6.64
Number of super-enhancer constituents: 35             
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_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_23750chr5:131812907-131814847Colon_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_39368chr5:131813131-131815907Jurkat
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_66244chr5:131813131-131815907Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5131813702131813794
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
CAGGCTGCCC CTCTGGGCTG GCACAGGAGG GCAGGGGAGG GCCTTCCCTA AAGGAAGCCT 60
GCAGGTGAAT CCCAGCGCCC GCCTGATGTA AGGTGGCAAC TGGCCAGCAG CCAGAGGTGC 120
CAGGTGTTCT CAGGGATCAA GAAACCAGGA ATTAGGCCCA CCAGAGCCAT AGGGTCTGAC 180
CCGAGCCTGG TGGCTGGGAA TGAGAATGCA TCTGTGCATG GTCCTGAGTC TCACAGCCAT 240
CCAGGGTCCA GACCTCTGAG GAACTCCAGG ACCCAACAGA GGGTCTGGTT TAAAGCAGAA 300
CAGGAGACTA GGTTGTCTTG CTGAGACAGA AACATGGCTA AAAAGTCCTC TTTGATCCTG 360
GGAGCTGAGA TAAGGCCTAG CAGGCCAGAG TCCCCCGTTT GCTCCAAACA GGCCTGGTGT 420
GGCCAAGCTG CCCCCTGCAC TGAGGCCAAG TTACAAGCCT GTCTGTGTCT CGGCCCCCTG 480
GGGCCCCACC CTTCGAAACT GCAGGTGGCC TCCAGGGCAT AGGTGGGGCA AACCCTACCC 540
TGTTGGGGCC CTGGGGCCTG TAGCGGCAGA GCCATGTTGC CAGGGGTGTT GGAAGGTGTG 600
TGTGCTGGGG GAAGGGAGGA GAGCTGAAGG CAGGGCAGCA CAGCAGCTGC AGCTTTTGCC 660
GCCTTCCCTC AGCATCCACA AGTGCTTGCT TGGCATAAGG TGCTCGGGCC CTGCCCCTTG 720
CTAGCTCTCC CCAGCTTCTT GTGCAGGCCT CCGTGTTCTT CTCTCAGGCA GCCTGATATG 780
GAACCAACCT GGATTCTGGG CACAGATAGA TGATGTGGGT TGGAACCAAG GCTCCATACT 840
GATTAGGTGG TGAGAGTTGG TTTCCTGGTC TGTGAACAAG GGCCGTGGTG GGGTGCCAGT 900
GCCGTGGTAC ACACGTGGTG CTTGGCATAG CACCCAGCAC AAAGTGAGCA CTCGAGGCCT 960
GTGTTGCCAT TATCCAGCCA CACTTTGAGG TCTTTTCCAG TTCTGCTCAT TTGTGAGCTT 1020
GTGGGATCAT CTCCTTGGGT GAGGAATGGT GGGCTGGACG TCTGCCTCCC CTCTTTCATT 1080
CAGTCCCCAT GTCCTTGCTC CATAGCCTCC 1110