EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-12936 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr17:55955200-55956970 
Target genes
Number: 9             
NameEnsembl ID
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
ATCCCAGTGC ACTCCAGCCT GGATGACAGA GTGAGACTCC GACTCAAAAA AAAAAAAAAA 60
AAAAGTCAAA GAAAGGAAAA TCATTTAGCC CAGGGCTCTG TGATCTATCC CAGGCTGCAA 120
GTCCTGCCTA GGTCTCACCC AGACCCACCC ACTCATTCCC CACCTCCCAC TCCAGTACAG 180
CCTGCCAGCT CCTGGTACCA CTCGTGACAA AGATCCCAGC TCTGTTCCTG TCCCTGACTC 240
AAAACACTTC CCTCCCTCCT CCCCTCAGTA ACTTTCTAGG ACTCTATGAG CTCCGTAAGC 300
TGCAATCACA GAGACTTTTC TCATTCGGGA GGTGACAGGA CACAGCAGTG AAGAGTGATT 360
AGCTTTAAGT CAGAATGACC TGGATTCGAA CTCCAGCTCT TAGTCTTGGG GAAGTTATGA 420
AATCTCTCAA GGCTCAGTTT CCTCGTCCAT AAATAGGGGT GATGACAACA GTGCCCGCCT 480
CTGCATTAAA TGTGATGGTG TAGGTAAAGA ACCTGCTCCG TTTCTGGCAT TGGAAGGGTG 540
CTTAGTCAAT GCTAGCTACA CTTGTATGAT AACAGAGTTC ACCACTGCTC TGGGGCTGTT 600
CTGGGGAGAA GGGAAGATCT AACTGGGACA GGTGCCCTGT CCCATCATCT CCCCACCCCC 660
TCACCACTCC AGGCCTGAGC CATTCTAAGA AACAGCAGCT CTAGGGCAAA GAGGTCACAC 720
CCCAGCTCCA GCAGCCCCAG CACAAATGTG GAGCCCAGAA AAACAAGCAC CCCGGAGACC 780
CATGGGATCT TCCTGGCAAC TACCTTGATT ATTTATTTAT TTATTTATTT ATTTATTTAT 840
TTATTTACTG AGAGTCTCAC TCTGTCACCC AGGCTGGAGT GCAGTGGCAC CATCTTGGCT 900
CACTGCAACC TCCGCCTCCG GGGTTCAAGC GGTTCTCCTG CCTCAGCCTC CCAAGTAGAT 960
GGAATTACAG GCATGCGCCA CCACCCCTGG CTAATCTTTG TATTTTTAGT AGAGATGGGG 1020
TTTCACCATG TTGGCCAGAC TGGTCTTGAA CTACTGACCT CAAGTGATCC ACCCACCTTG 1080
GCCTCCCAAA GTGCTGGGAT TACAGATGTG AGCCACTGTG CCCAGCCTAG CTTCATTTTA 1140
AGCTTCCAAA TTACAGAGTC TCTAACCTGG AAGAAGTTTC CAGGGACCTT GCAGTCTACC 1200
TCCCTGCCTC CAGTTATCAA ACTACCTTAA TGAAAGAGAC TTGCTCTCAT TGCTTAAAAA 1260
TCCTCACAAT ATCCCTAGCC CAAGGATGGC AGCTAGCCAT TCCATCAATT ACTGATGACT 1320
GGCTGGGAAT GCTGTGTTCT GTGTTAAGGA GGATCTGAGG CTCTGTCTTG ACTCAGCAGG 1380
AAAGAGCACA GTGATGAATC AGCCATGTTT GCTGTGGGCT TGGGAGGGGA AGTGCCAATA 1440
CACATTCCCT GTTTGTCATT CCTACTCTGG CATCTCCCTT GACTATAAGC TCCCAGAAAG 1500
CAGAGGCTGA GCTTTACTTA ACTCTGTGTC CCATATGGTA CCAGACATAC CGCCTAGCCT 1560
AGAGTAGGAA TTTAGGAAAT GTTTGCTCTT GCAATCCTTA CATTTTGCAA GTTCTCCTTG 1620
GTATCTAGCT AAAATGTCTC TTGCTGCAGT AGAAGCCTGT TCTTTGAAAT ATACTGAGCA 1680
GTCCAGCCAA GTTTCGTGTT GTTTGTACAC AGCCCCAGCC ACTGATCCTC TTCCCTGCCA 1740
CCCTGTGCTC TGAGACATGA CAGATTCTCA 1770