EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS128-10401 
Organism
Homo sapiens 
Tissue/cell
MCF-7 
Coordinate
chr18:74766250-74767440 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ATF3MA0605.2chr18:74766744-74766756GGTGACGTCACC+6.22
ATF3MA0605.2chr18:74766744-74766756GGTGACGTCACC-6.22
CREB1MA0018.3chr18:74766744-74766756GGTGACGTCACC+7.22
CREB1MA0018.3chr18:74766744-74766756GGTGACGTCACC-7.22
Klf1MA0493.1chr18:74766344-74766355AGCCACACCCA+6.14
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_02301chr18:74765615-74769291Astrocytes
SE_03187chr18:74763012-74767105Brain_Angular_Gyrus
SE_03187chr18:74767106-74767924Brain_Angular_Gyrus
SE_03925chr18:74762993-74769676Brain_Anterior_Caudate
SE_04802chr18:74760877-74769887Brain_Cingulate_Gyrus
SE_05798chr18:74762601-74769949Brain_Hippocampus_Middle
SE_06694chr18:74761722-74769901Brain_Hippocampus_Middle_150
SE_07751chr18:74762635-74769942Brain_Inferior_Temporal_Lobe
SE_08838chr18:74766101-74766370Brain_Mid_Frontal_Lobe
SE_08838chr18:74766418-74766616Brain_Mid_Frontal_Lobe
SE_09139chr18:74763390-74771272CD14
SE_10547chr18:74764261-74769635CD19_Primary
SE_11015chr18:74762704-74785115CD20
SE_12115chr18:74764048-74769337CD3
SE_13103chr18:74765655-74769275CD34_Primary_RO01480
SE_13673chr18:74763883-74769625CD34_Primary_RO01536
SE_14260chr18:74763782-74769393CD34_Primary_RO01549
SE_15038chr18:74763788-74768613CD4_Memory_Primary_7pool
SE_15651chr18:74764917-74768462CD4_Memory_Primary_8pool
SE_16468chr18:74765452-74768807CD4_Naive_Primary_8pool
SE_17255chr18:74765526-74769066CD4p_CD225int_CD127p_Tmem
SE_17959chr18:74762819-74769776CD4p_CD25-_CD45ROp_Memory
SE_18700chr18:74763026-74769998CD4p_CD25-_Il17-_PMAstim_Th
SE_19374chr18:74763980-74769767CD4p_CD25-_Il17p_PMAstim_Th17
SE_19981chr18:74763553-74769915CD56
SE_21261chr18:74765053-74769077CD8_Memory_7pool
SE_22307chr18:74763553-74769856CD8_primiary
SE_25341chr18:74763020-74769931DND41
SE_25885chr18:74765504-74769852Duodenum_Smooth_Muscle
SE_26884chr18:74764538-74766920Esophagus
SE_30168chr18:74765890-74769751Fetal_Muscle
SE_34994chr18:74765147-74769503HeLa
SE_39197chr18:74765915-74769297IMR90
SE_41189chr18:74765691-74769624Left_Ventricle
SE_42218chr18:74764253-74769817Lung
SE_47137chr18:74764303-74771360Panc1
SE_48227chr18:74765445-74769622Psoas_Muscle
SE_49182chr18:74765702-74767536Right_Atrium
SE_50626chr18:74764327-74769788Sigmoid_Colon
SE_51089chr18:74763882-74771359Skeletal_Muscle
SE_52417chr18:74764263-74769800Small_Intestine
SE_53332chr18:74764213-74769843Spleen
SE_58547chr18:74756065-74865317Ly1
SE_61817chr18:74764079-74793826Toledo
SE_62620chr18:74763866-74793718Tonsil
SE_65574chr18:74763757-74769532Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr187476660274767022
Number: 1             
IDChromosomeStartEnd
GH18I077051chr187476336674770955
Enhancer Sequence
GTGGGAGATG TCAACGAGAA GGGACATGGA GCGAAGAGCT CACCCCCGGA TATCTGGGCA 60
AGAGACTTAA GGAGGAGGGC AGAGCTTGTG CTTCAGCCAC ACCCAGGAGG CTGCGGGAGG 120
GAGGGGCCGC AGGAGATGTG GTTGGAGAGG CCCCTGGGGA ACAGGTGGAG GGGATTTGAG 180
CAGGGAGCGA GGTGCTCAGC AGCTAGCTGG CAGGGAGAAC CAACAGGGAT GGATCAGGAT 240
GGAGGCTGGG ACCCACTTAA TCACCCAGGT GGGCAGAGGA GGGCTTGGGC CTTGGTGATG 300
GGAGAGGTGC TTGCTAAGTA TCAGAGCTTC CCTGGGTCCT TGGCACAATC AGCCATCAGT 360
GCTCTCAGCA AAGACATAGA AATAGTGCTC CTCATTTTGT ACCTGGATAA GGGGAGAGCT 420
CAAGTTCCAA TCCCTGTTAG CGGCGGGTGA CACAACCATG CACACATCTC AAATTCCAAT 480
TCCTGTTAGC GGCGGGTGAC GTCACCATGC ACACATCTCA AGTTCCAGTT CCTGTTAGCG 540
GTGGGTAATG TCACCATGCA CACATCCTGT TTTCTCCTGC TCTGCCACTG TGATCTCCAG 600
ATGATCAATT TCATATTATC AGGAAAATGA CCTTTGGCAC AGAAAGCCCA GAGGAGAAGG 660
TGAGGGACTT GCATGCACGC ACACATTTAA ATGTCAACAT TCTATGGAAT TCAGTATCAT 720
AAAGGTATGC AAACCATGGG AAGTAATCAT GAGTTTGCTC TGGGAGGCCC CGCAGTTAGA 780
AGGGAACCTT CTGGGCACGC ACATCGTGGA TGGAGACAGA GGAACGGCAG CGCCGCCTGC 840
TGCTGCTGGG CCCTGCGTGT CTGTACCACC TTCTGTGGTA GAGAAAACAG CAGGCGGCTT 900
TGCTGCAAAC TCCAGCACAG CCTCTGTGTG GGAGGAGCAG GGTCAGCAGA AACCCAGAGG 960
CAGGAAGGAG CTGAGCTGAG CTGGTGCAAG AGTGTCCTGC CCTGGGAGGA AGTGGCTTTG 1020
TACCAACTGA TAAAATGCCC AGAGTAGGGG GCACATAACT GTAAACTTCT AGAACCCACA 1080
TCCTCAAAGC CCAACCCCTG ACCCAGGAGG TGCATGGGTG GCTGTTCCCT CCCAGCCCAG 1140
TGCCACCTCT GCCATCCTCC CTGGCTGGGA AAGATGAACT GCGCTTAAAA 1190