EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS052-17922 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr18:74819140-74821450 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MNX1MA0707.1chr18:74820346-74820356GGTAATTAAA+6.02
Stat4MA0518.1chr18:74819431-74819445CTTCCAGGAAACAA+6.37
ZNF263MA0528.1chr18:74819363-74819384CGTTTCTCACCCTCCTCCTCC-6.79
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_02611chr18:74819139-74821219Astrocytes
SE_09139chr18:74806175-74829571CD14
SE_11015chr18:74809799-74821940CD20
SE_12122chr18:74816496-74821102CD3
SE_13574chr18:74819745-74821023CD34_Primary_RO01536
SE_14365chr18:74819530-74821024CD34_Primary_RO01549
SE_15148chr18:74810251-74821398CD4_Memory_Primary_7pool
SE_16599chr18:74816619-74821191CD4_Naive_Primary_8pool
SE_17992chr18:74810218-74822100CD4p_CD25-_CD45ROp_Memory
SE_18533chr18:74809958-74822708CD4p_CD25-_Il17-_PMAstim_Th
SE_19370chr18:74810542-74821336CD4p_CD25-_Il17p_PMAstim_Th17
SE_19981chr18:74797810-74821764CD56
SE_22307chr18:74808493-74829791CD8_primiary
SE_25341chr18:74808379-74829893DND41
SE_25885chr18:74818246-74821597Duodenum_Smooth_Muscle
SE_26884chr18:74819058-74821415Esophagus
SE_30168chr18:74818848-74821143Fetal_Muscle
SE_31917chr18:74819050-74819722Gastric
SE_31917chr18:74819839-74820324Gastric
SE_32648chr18:74818820-74820946GM12878
SE_37921chr18:74818150-74821837HSMMtube
SE_39287chr18:74818724-74821536IMR90
SE_39556chr18:74818703-74819650Jurkat
SE_41189chr18:74818763-74819822Left_Ventricle
SE_41189chr18:74819851-74821541Left_Ventricle
SE_42218chr18:74818731-74821599Lung
SE_44218chr18:74818589-74821593NHDF-Ad
SE_47137chr18:74808444-74829846Panc1
SE_48227chr18:74819069-74821504Psoas_Muscle
SE_49182chr18:74819153-74821270Right_Atrium
SE_50555chr18:74817663-74821942Sigmoid_Colon
SE_51089chr18:74812396-74822600Skeletal_Muscle
SE_52417chr18:74817702-74821504Small_Intestine
SE_53332chr18:74817542-74821683Spleen
SE_58547chr18:74756065-74865317Ly1
SE_62520chr18:74808577-74846347Tonsil
SE_65574chr18:74818836-74819850Pancreatic_islets
SE_66494chr18:74818703-74819650Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr187481927674819721
Number: 1             
IDChromosomeStartEnd
GH18I077094chr187480680074829611
Enhancer Sequence
GAGCTGGTCT ATTCAAAGCT AAACACAGGC AAAAACAGGT AACTTCCTTT AGTTAAGGTT 60
GACAACTTGG ACCTTTGGGG GCATTTTGCC CATCCAGACA TAAATGAACC TCCTATCACC 120
GGCTGTGTTC TCCAAGTGCC TGTTCCTGGC CCAGGCATCA TCTCATCTCT GCCTCCTGTG 180
AGCCCTCGCC TGCCCAGTCC CCTTCCTGTT CCCTGGCTCT ATCCGTTTCT CACCCTCCTC 240
CTCCCACCTC CTTATGCTGG GACTAGGCAA ACACAAATGC AACACTCACT CCTTCCAGGA 300
AACAAAGCTC CAAGGACTTG TCCCAAATCA GAATAGTGTG GGCCATGTAA ATATTTTGGG 360
ACTTGCTGGT AGACAAAGAG AGCTATTTTT GGGCAAGGGG CTCTTGAACG CAGCTGAAAT 420
CTGTCCACAA GGTGCTGAAC TGCTCCTTGG AGAGGGGCCA TGTTTCTTCC GAATCAGTTT 480
GTTCTGATCA AATGTTGTCA TGCTTCATAG CACAACTCTA GGTTACGCTT GGGATGATTG 540
ATCTTAATCA TGATTTAGAA AACTCAAGAA TACTGGACAC AGAATTGGTG AAAATAACTC 600
AAGTCCAGAT CAGACTTTTG AATACATCTT GTTGGATTTG ACTAGTTAGA CAAGCCTACT 660
TACTTGCATT TGACTGGCCT CTCAGATTAA TATAAAGAAT ATTTATATGA ATCACTGAGG 720
GTTGGTTAAT TCTAGCCTTA AATGCAAAAT TTATATACTA GCAGGAAAAG AAAGACAAGA 780
GGAACAAAAC GACAACTTGA TGTGTGGGAG CCCCCATCAG AGCCGTTAGT GGAAATGGCC 840
CCTGAGCACC GGTAAGTGAG ACGTGTCTCA AGGAACTATG GTGGGAACGA CAGAGCATCT 900
GGCTGATAAT CACGAGTGAC TGGCAGTCTG CCTTATTAGC TTCTGACACT CTGCCCCAGT 960
CTGCCTTTTA GAGAAGAGCT CGAGAAGGAT GAAGCTCTCA CTGTCACGGG GCTAAGAGCT 1020
CAGCCTGGCA GCTGGTTTCT GTAATGTGCT GAAAAGATCC ATCTGCACAC AAAAGCAGCT 1080
GCATGCTTGG AGGAAATCTT TTTTATTTCA TTTTTTGCAA TTAATCAAAT TGAGAGAGCC 1140
AGAGAAAAAT TGGGTAAACA TGTGAAATGC TGCAAGGAAA GTCAGCTGAC TCTGAAGCAT 1200
CTCTTGGGTA ATTAAAGAAG CCTTTTGTAA ACTAATAGAA AAGGAAAGAG AGGGAGGAAG 1260
AACTGAGCTA GAGCTGTGGG AGGGACAGAC TTTCAGATTC CATCAGGACC GCTGAGACTT 1320
CCGCGGTCTC AGTTGGTATT CAGTTCTAGA TCCGATTTCC AGCCACTGGG ATGACTGGAC 1380
ACTTTGATAA TGTCTGTGTG ATTATCAACA CTTAGTGTTA CCTCGAGGGT TAACATTGGG 1440
CACAGGCAAA GTTAGTCACC CAGATTTACT AGGAAGCAGT CCACTGTTGT TGACTGTTAG 1500
GCTCTCGTTT TTAATAATGT ACACCTAAAG CAGCTTAGAC TACATGTCAC CTTGGTGGAA 1560
CCACAGGATA ATTCAGCATA GATAAAACTC ACTAGCCTAT CTGTGCAGGG AAATAGCTCC 1620
CAGCTGAAAT GCTGGGGAAC AAACACCTTG TTCCTAGGTA TTTTACTGAT TTCATTCTCT 1680
AGGTAGTTCT GACTTTCTAC GGTGAAAATC AGGCAGGTGA GACCTAGGTC TCAATCCAGG 1740
TTCCATCTGG GTGACCCCGA ACAAGACTCC ACTTTTCTGA GCCTCAGTTT CCCATAAAGT 1800
AGAGGTAATA AAACTTGCCT TTCTGCACTG GTGTGAGAAT GAAGCCCATG TGGGCTGCAG 1860
GGCTGGGCAG GGCTAGGGTT AGGGTTGGGG TATGCTGCAG GCGTTGCTTT GCTTTCTGTC 1920
TTCCTCTTAC CTCCACCAGG TCCAGGGTTC CCTGGGTGGG TGGTGAGCAG CTGCAGAAAC 1980
ATCGCTACCT ACTTACTATC ACACATGTTC AGAGACCTCT AGATGGCTTC CCACATCTAG 2040
ATGCATCCAC TCCTAAACTG ACAAGGTCAA GGGAAGAAAA AAGGCTAAAA ACACCAGCTG 2100
CCCAGAAGTT ACATCCTACA ATTGCCTGTC AACAAAGCTC TTGATCCAAC ACACACAACT 2160
GAAGCACAGG GGAAATGCAA CTGCTGCTGC TTTAAGACCA CACAAAGTGT CCTGGGGTGT 2220
GGAAGGTGAG GAAAGAGGGA AAAAAGTGAA GAGGAAGGAC ATTCACGAGA CAGCCATGCC 2280
CCAAACGCCA GACAAGTATT CAAATATTAA 2310