EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS178-19192 
Organism
Homo sapiens 
Tissue/cell
Skeletal_muscle 
Coordinate
chr5:131810150-131811350 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11741255chr5131811182hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr5:131810769-131810790GATGGAGGAGGGGGAAGGTAA+6.27
ZNF263MA0528.1chr5:131810303-131810324CCTTCTGCCTCCTCCTTCTTC-6.44
ZNF263MA0528.1chr5:131810772-131810793GGAGGAGGGGGAAGGTAAGGC+6.63
ZNF263MA0528.1chr5:131810766-131810787GGAGATGGAGGAGGGGGAAGG+6.65
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00037chr5:131810090-131812540Adipose_Nuclei
SE_01257chr5:131810577-131811720Adrenal_Gland
SE_04124chr5:131810599-131811590Brain_Anterior_Caudate
SE_06435chr5:131810039-131812439Brain_Hippocampus_Middle
SE_10915chr5:131798063-131818030CD20
SE_11856chr5:131806085-131811485CD3
SE_14495chr5:131805826-131811661CD4_Memory_Primary_7pool
SE_16304chr5:131807811-131811139CD4_Naive_Primary_8pool
SE_17370chr5:131804876-131811594CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131804786-131818044CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131805804-131811428CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131810146-131811550CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131797758-131816289CD56
SE_20775chr5:131810171-131811664CD8_Memory_7pool
SE_22284chr5:131797996-131818026CD8_primiary
SE_23079chr5:131810420-131815180Colon_Crypt_1
SE_23750chr5:131810479-131811551Colon_Crypt_2
SE_25340chr5:131808656-131817904DND41
SE_25784chr5:131810212-131813275Duodenum_Smooth_Muscle
SE_26597chr5:131810388-131811474Esophagus
SE_27629chr5:131808629-131817861Fetal_Intestine
SE_28559chr5:131808476-131817875Fetal_Intestine_Large
SE_30917chr5:131809910-131811467Fetal_Thymus
SE_31393chr5:131810363-131811622Gastric
SE_39368chr5:131809998-131811728Jurkat
SE_40726chr5:131809980-131815612Left_Ventricle
SE_42103chr5:131809951-131815230Lung
SE_48659chr5:131810417-131814893Right_Atrium
SE_50023chr5:131810017-131811707RPMI-8402
SE_50051chr5:131808593-131816260Sigmoid_Colon
SE_52336chr5:131808690-131816220Small_Intestine
SE_53285chr5:131809900-131816337Spleen
SE_54554chr5:131810068-131812535Stomach_Smooth_Muscle
SE_55171chr5:131810920-131811233Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131810440-131811582Pancreatic_islets
SE_66244chr5:131809998-131811728Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5131810202131811200
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
TCCTGGGGGC TCTAGTGGAG AATCCCTTTC CTTCCTTTCC CTTTCCAGCT TTTAGAGGCT 60
GCCTGCATTC CTTGGCCTGC AACCCCTTCC TCCACTTTCA AAGCCAGCAC TGGCTGGTCA 120
GGTTTTTCAC AATGCGATCT CTCTGGTTCT GACCCTTCTG CCTCCTCCTT CTTCATTTAA 180
GAACCCTTGT GATTACACTG GGCCCACACC AATAATCCAG GGTAATCTCT CTATTTGCAA 240
GTGAGCTGGT TAGCAACCTT AATTCCATCT GCAGTTTTAA TTCCTCTTTG CCATGTAGCA 300
ACATATTCAT AGGCTCATGC ATTAGGACGT GGACCTCTTT ATTCCACTGT GGACCAATAC 360
TCTGCCTTCC ACACCTAGCC TCTCTTCTGA GTTTTCCAAG GGCCCCCCAT CCTCAGGCAT 420
CCTCAGGCAT AGACAGCCGG CTGGGCCAGA CCACAGTCAG GATGTTCCCG CCACTATCAG 480
AGAGGTCCTT TCTACCTAAG TCCCCTCCCA CCTGCCTGCT CCTCTTTCAG CTCGGTCTGT 540
CCTGGATTCC TCTTCCTTCA TCCTCTGCTC CCAGTCTTAG GTAGAGAAGA GCTGAGCAGG 600
AAGTGCCAGG GGGTGTGGAG ATGGAGGAGG GGGAAGGTAA GGCCTGAGGC ACCAGGGCTC 660
TGGGAGCCCA GGGAGCTGAG GCCTTTCAAT CCAGACACCC TGCACTTCTC TGGCTCTGGG 720
GCCTCTGGGG ACCACACACT CAGCTCCAGG GCTGGAGGGG TGGCCAGCCA AGTATTGGAA 780
CCCTTCTGCT TGTACATCCC TAGCTGCCCT TAACAGCCAC AGTTCACCTG GCCCTTTTCT 840
TGGGTGATGA CAGACTGTCT GCCTTAATTT ATTCCCTTTC CCCTGTCCCT CCCTAGGCCT 900
CAGGCTGGAA CTTTCAGGAG CTTCCACGGG AGGCAAGGCC CCAGCCAGGC CTCTGTCCCT 960
GGGCTGCTTG GTGTGGGGAT GGGGGATCCA GAACCCCAGC AGGAGGGCAG ATGGGGAGCA 1020
CAGGGCAGGA GGGGCAGGAC AAAGCCTTTG GCCCTCAGGG AGGGTGACCA ACTGGCCCTG 1080
GTTTGCCTGG GACTTTCCCA GTTTTAGCAC TGAAAGTCCC AAATCCTGGG AAACTCCTCA 1140
GTCCTAAGCA AACTGGAACA GTTGGTCAGC CTATCTCCAA GCCTTTTGCA CCTCCTAATC 1200