EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS052-16408 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr17:55955180-55956970 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr17:55955445-55955463ACTTCCCTCCCTCCTCCC-6.05
Nr2f6(var.2)MA0728.1chr17:55956246-55956261TGAACTACTGACCTC-6.07
RARAMA0729.1chr17:55956243-55956261TCTTGAACTACTGACCTC-6.1
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_03878chr17:55950042-55956010Brain_Anterior_Caudate
SE_03878chr17:55956245-55959769Brain_Anterior_Caudate
SE_04783chr17:55943537-55956092Brain_Cingulate_Gyrus
SE_04783chr17:55956096-55961004Brain_Cingulate_Gyrus
SE_06590chr17:55943471-55960413Brain_Hippocampus_Middle
SE_07738chr17:55949624-55958078Brain_Inferior_Temporal_Lobe
SE_25794chr17:55954886-55959515Duodenum_Smooth_Muscle
SE_27772chr17:55956423-55959989Fetal_Intestine
SE_28796chr17:55956222-55960267Fetal_Intestine_Large
SE_29569chr17:55956183-55960712Fetal_Muscle
SE_31404chr17:55956470-55957264Gastric
SE_33448chr17:55950667-55958164H2171
SE_34179chr17:55956198-55957251HCC1954
SE_34254chr17:55956128-55959730HCT-116
SE_35331chr17:55956169-55958233HepG2
SE_37539chr17:55955227-55958306HSMMtube
SE_38977chr17:55956158-55960130IMR90
SE_40601chr17:55950532-55956029Left_Ventricle
SE_40601chr17:55956187-55959902Left_Ventricle
SE_42102chr17:55955210-55956014Lung
SE_42102chr17:55956229-55960103Lung
SE_44235chr17:55955071-55959711NHDF-Ad
SE_44887chr17:55955168-55955961NHLF
SE_44887chr17:55956016-55959576NHLF
SE_46579chr17:55955153-55959649Osteoblasts
SE_47384chr17:55950105-55960103Panc1
SE_48056chr17:55955055-55960204Psoas_Muscle
SE_51111chr17:55956084-55960134Skeletal_Muscle
SE_52082chr17:55956033-55957874Skeletal_Muscle_Myoblast
SE_52598chr17:55956285-55957177Small_Intestine
SE_54487chr17:55943323-55956053Stomach_Smooth_Muscle
SE_54487chr17:55956104-55960313Stomach_Smooth_Muscle
SE_56380chr17:55955156-55957753u87
SE_63290chr17:55922884-55976538NCI-H82
SE_63875chr17:55955581-55957945HSMM
SE_65273chr17:55954898-55955555Pancreatic_islets
SE_65273chr17:55955619-55956425Pancreatic_islets
SE_65273chr17:55956549-55957557Pancreatic_islets
SE_67933chr17:55955156-55957753u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr175595530855955557
Number: 1             
IDChromosomeStartEnd
GH17I057877chr175595526755960716
Enhancer Sequence
GGTTGCAGTG AACAGAGATA ATCCCAGTGC ACTCCAGCCT GGATGACAGA GTGAGACTCC 60
GACTCAAAAA AAAAAAAAAA AAAAGTCAAA GAAAGGAAAA TCATTTAGCC CAGGGCTCTG 120
TGATCTATCC CAGGCTGCAA GTCCTGCCTA GGTCTCACCC AGACCCACCC ACTCATTCCC 180
CACCTCCCAC TCCAGTACAG CCTGCCAGCT CCTGGTACCA CTCGTGACAA AGATCCCAGC 240
TCTGTTCCTG TCCCTGACTC AAAACACTTC CCTCCCTCCT CCCCTCAGTA ACTTTCTAGG 300
ACTCTATGAG CTCCGTAAGC TGCAATCACA GAGACTTTTC TCATTCGGGA GGTGACAGGA 360
CACAGCAGTG AAGAGTGATT AGCTTTAAGT CAGAATGACC TGGATTCGAA CTCCAGCTCT 420
TAGTCTTGGG GAAGTTATGA AATCTCTCAA GGCTCAGTTT CCTCGTCCAT AAATAGGGGT 480
GATGACAACA GTGCCCGCCT CTGCATTAAA TGTGATGGTG TAGGTAAAGA ACCTGCTCCG 540
TTTCTGGCAT TGGAAGGGTG CTTAGTCAAT GCTAGCTACA CTTGTATGAT AACAGAGTTC 600
ACCACTGCTC TGGGGCTGTT CTGGGGAGAA GGGAAGATCT AACTGGGACA GGTGCCCTGT 660
CCCATCATCT CCCCACCCCC TCACCACTCC AGGCCTGAGC CATTCTAAGA AACAGCAGCT 720
CTAGGGCAAA GAGGTCACAC CCCAGCTCCA GCAGCCCCAG CACAAATGTG GAGCCCAGAA 780
AAACAAGCAC CCCGGAGACC CATGGGATCT TCCTGGCAAC TACCTTGATT ATTTATTTAT 840
TTATTTATTT ATTTATTTAT TTATTTACTG AGAGTCTCAC TCTGTCACCC AGGCTGGAGT 900
GCAGTGGCAC CATCTTGGCT CACTGCAACC TCCGCCTCCG GGGTTCAAGC GGTTCTCCTG 960
CCTCAGCCTC CCAAGTAGAT GGAATTACAG GCATGCGCCA CCACCCCTGG CTAATCTTTG 1020
TATTTTTAGT AGAGATGGGG TTTCACCATG TTGGCCAGAC TGGTCTTGAA CTACTGACCT 1080
CAAGTGATCC ACCCACCTTG GCCTCCCAAA GTGCTGGGAT TACAGATGTG AGCCACTGTG 1140
CCCAGCCTAG CTTCATTTTA AGCTTCCAAA TTACAGAGTC TCTAACCTGG AAGAAGTTTC 1200
CAGGGACCTT GCAGTCTACC TCCCTGCCTC CAGTTATCAA ACTACCTTAA TGAAAGAGAC 1260
TTGCTCTCAT TGCTTAAAAA TCCTCACAAT ATCCCTAGCC CAAGGATGGC AGCTAGCCAT 1320
TCCATCAATT ACTGATGACT GGCTGGGAAT GCTGTGTTCT GTGTTAAGGA GGATCTGAGG 1380
CTCTGTCTTG ACTCAGCAGG AAAGAGCACA GTGATGAATC AGCCATGTTT GCTGTGGGCT 1440
TGGGAGGGGA AGTGCCAATA CACATTCCCT GTTTGTCATT CCTACTCTGG CATCTCCCTT 1500
GACTATAAGC TCCCAGAAAG CAGAGGCTGA GCTTTACTTA ACTCTGTGTC CCATATGGTA 1560
CCAGACATAC CGCCTAGCCT AGAGTAGGAA TTTAGGAAAT GTTTGCTCTT GCAATCCTTA 1620
CATTTTGCAA GTTCTCCTTG GTATCTAGCT AAAATGTCTC TTGCTGCAGT AGAAGCCTGT 1680
TCTTTGAAAT ATACTGAGCA GTCCAGCCAA GTTTCGTGTT GTTTGTACAC AGCCCCAGCC 1740
ACTGATCCTC TTCCCTGCCA CCCTGTGCTC TGAGACATGA CAGATTCTCA 1790