EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS155-06767 
Organism
Homo sapiens 
Tissue/cell
Ovary 
Coordinate
chr18:74819150-74820810 
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
ATTCAAAGCT AAACACAGGC AAAAACAGGT AACTTCCTTT AGTTAAGGTT GACAACTTGG 60
ACCTTTGGGG GCATTTTGCC CATCCAGACA TAAATGAACC TCCTATCACC GGCTGTGTTC 120
TCCAAGTGCC TGTTCCTGGC CCAGGCATCA TCTCATCTCT GCCTCCTGTG AGCCCTCGCC 180
TGCCCAGTCC CCTTCCTGTT CCCTGGCTCT ATCCGTTTCT CACCCTCCTC CTCCCACCTC 240
CTTATGCTGG GACTAGGCAA ACACAAATGC AACACTCACT CCTTCCAGGA AACAAAGCTC 300
CAAGGACTTG TCCCAAATCA GAATAGTGTG GGCCATGTAA ATATTTTGGG ACTTGCTGGT 360
AGACAAAGAG AGCTATTTTT GGGCAAGGGG CTCTTGAACG CAGCTGAAAT CTGTCCACAA 420
GGTGCTGAAC TGCTCCTTGG AGAGGGGCCA TGTTTCTTCC GAATCAGTTT GTTCTGATCA 480
AATGTTGTCA TGCTTCATAG CACAACTCTA GGTTACGCTT GGGATGATTG ATCTTAATCA 540
TGATTTAGAA AACTCAAGAA TACTGGACAC AGAATTGGTG AAAATAACTC AAGTCCAGAT 600
CAGACTTTTG AATACATCTT GTTGGATTTG ACTAGTTAGA CAAGCCTACT TACTTGCATT 660
TGACTGGCCT CTCAGATTAA TATAAAGAAT ATTTATATGA ATCACTGAGG GTTGGTTAAT 720
TCTAGCCTTA AATGCAAAAT TTATATACTA GCAGGAAAAG AAAGACAAGA GGAACAAAAC 780
GACAACTTGA TGTGTGGGAG CCCCCATCAG AGCCGTTAGT GGAAATGGCC CCTGAGCACC 840
GGTAAGTGAG ACGTGTCTCA AGGAACTATG GTGGGAACGA CAGAGCATCT GGCTGATAAT 900
CACGAGTGAC TGGCAGTCTG CCTTATTAGC TTCTGACACT CTGCCCCAGT CTGCCTTTTA 960
GAGAAGAGCT CGAGAAGGAT GAAGCTCTCA CTGTCACGGG GCTAAGAGCT CAGCCTGGCA 1020
GCTGGTTTCT GTAATGTGCT GAAAAGATCC ATCTGCACAC AAAAGCAGCT GCATGCTTGG 1080
AGGAAATCTT TTTTATTTCA TTTTTTGCAA TTAATCAAAT TGAGAGAGCC AGAGAAAAAT 1140
TGGGTAAACA TGTGAAATGC TGCAAGGAAA GTCAGCTGAC TCTGAAGCAT CTCTTGGGTA 1200
ATTAAAGAAG CCTTTTGTAA ACTAATAGAA AAGGAAAGAG AGGGAGGAAG AACTGAGCTA 1260
GAGCTGTGGG AGGGACAGAC TTTCAGATTC CATCAGGACC GCTGAGACTT CCGCGGTCTC 1320
AGTTGGTATT CAGTTCTAGA TCCGATTTCC AGCCACTGGG ATGACTGGAC ACTTTGATAA 1380
TGTCTGTGTG ATTATCAACA CTTAGTGTTA CCTCGAGGGT TAACATTGGG CACAGGCAAA 1440
GTTAGTCACC CAGATTTACT AGGAAGCAGT CCACTGTTGT TGACTGTTAG GCTCTCGTTT 1500
TTAATAATGT ACACCTAAAG CAGCTTAGAC TACATGTCAC CTTGGTGGAA CCACAGGATA 1560
ATTCAGCATA GATAAAACTC ACTAGCCTAT CTGTGCAGGG AAATAGCTCC CAGCTGAAAT 1620
GCTGGGGAAC AAACACCTTG TTCCTAGGTA TTTTACTGAT 1660