EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-84249 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chrX:12993290-12994360 
Target genes
Number: 3             
NameEnsembl ID
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_09612chrX:12988035-12998325CD14
SE_10462chrX:12988094-12994898CD19_Primary
SE_11231chrX:12985204-12999646CD20
SE_11864chrX:12988038-12994643CD3
SE_14440chrX:12987980-12998536CD4_Memory_Primary_7pool
SE_15419chrX:12987940-12997781CD4_Memory_Primary_8pool
SE_15857chrX:12988349-12997348CD4_Naive_Primary_7pool
SE_16331chrX:12987867-12998136CD4_Naive_Primary_8pool
SE_16908chrX:12990950-12994997CD4p_CD225int_CD127p_Tmem
SE_17382chrX:12984499-13005297CD4p_CD25-_CD45RAp_Naive
SE_17855chrX:12984353-12998827CD4p_CD25-_CD45ROp_Memory
SE_18339chrX:12984154-13005741CD4p_CD25-_Il17-_PMAstim_Th
SE_19260chrX:12987945-12994944CD4p_CD25-_Il17p_PMAstim_Th17
SE_20114chrX:12987977-12994938CD56
SE_20864chrX:12990985-12998172CD8_Memory_7pool
SE_21563chrX:12990973-12997433CD8_Naive_7pool
SE_21967chrX:12987852-12998699CD8_Naive_8pool
SE_22410chrX:12987908-12994748CD8_primiary
SE_25447chrX:12988084-12998545DND41
SE_27537chrX:12991071-12994794Esophagus
SE_28103chrX:12991738-12997624Fetal_Intestine
SE_29081chrX:12991902-12997700Fetal_Intestine_Large
SE_30940chrX:12988069-12998536Fetal_Thymus
SE_31989chrX:12990943-12994855Gastric
SE_32462chrX:12991010-12998477GM12878
SE_38726chrX:12990952-12998013HUVEC
SE_39711chrX:12988437-12993732Jurkat
SE_39711chrX:12993783-12994484Jurkat
SE_49904chrX:12988074-12993756RPMI-8402
SE_50189chrX:12991006-12994726Sigmoid_Colon
SE_52563chrX:12990979-12994722Small_Intestine
SE_53489chrX:12988185-12995758Spleen
SE_55209chrX:12991031-12994682Thymus
SE_58191chrX:12993165-12994536VACO_9m
SE_58417chrX:12964783-13034394Ly1
SE_58905chrX:12964721-13049077Ly3
SE_60593chrX:12964761-12998409DHL6
SE_61870chrX:12964787-12998403Toledo
SE_62231chrX:12964510-13049336Tonsil
SE_66386chrX:12988437-12993732Jurkat
SE_66386chrX:12993783-12994484Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chrX1299360012994000
Enhancer Sequence
AGCCCCAGGG CCCCTGCCTC CTTCCTCCTG CCGTCCTGCC TCCGTCCCCG CCCTTTCATC 60
ATCCGCGTCC CTGTGAAGGC ATTCCCTAAA TCCGAGCCCG AGTGGTTCTC CCCGGGAAGG 120
CTACTTTGGG GAGCTGGGGG GATGCGAAAC ACCCTAGATA CTGGATAATG GGGTGGGGAA 180
ATCGATGATT TAAGAACAAA ACCGAAAAAC TGGCGTTTTG CCGTGCCGCT CGGAGGGGAC 240
ATTAAAAAAT TTCTTAGTGT TTGCCCGCAA AGGTATTGTG CGTTGCCTTG GAGGCTGAGA 300
TATGGGGGAA TAGACAAGTC CTTTGTTCTG AGGTTCATCT TCCGAGCCCC GAGCCTCCTC 360
CCAGCCTCGG ACGGCTGCGC GGGCTGCATC TGTGCAGCCT GGCGGCGGCG GGGCTGTGCT 420
ATGACATCTT TACAGTCCTT CTTGCAGAGA CATGTGTGCC AGGGATGCCG AATTGCCGGG 480
AGAGCAGGCA AGACCGGCTT CGGGGCGCGC GGCGGCCGCT TTGTGTGCGG GGCTGCATTG 540
TGACGCGGGC GATGAAGCCG GTAGGGCGGT GGTCGGAAGC TCCAGCCGCG GCCGCCGCCT 600
TTGTGAGAGG ACTAGAAAGC CGGATCCGGC CCGCATCCTT GCGGAGAGGC CGCGGCTAGG 660
AAATGGAAAC GCTTTTCCTA CCTGGGCTCC ATTTTAGGAA TTCTTGCCGA TTTTTCCCAC 720
TTGAATTTGG AAGTGGCTTT CCTCTTCTTT CCTTGTCCTA GCCAGCCTTT AATTTTAAAC 780
GCTGTAATTA ACAATTCGCA GTGGTCAATT TCCTTTATTC TGCAAGATTC GGCTTTGAGA 840
GGCATCCGCC CTCTTTGGTC CACAGCGTTT TGAAATATGG GGAGGAGGGG CGCGGGGGGT 900
GTCGCCTCTT TTTCTGTAGA AAGAGGAAGC TCGTGAGCGC GGAACGGCAG CAGTAGGAGA 960
GCGAGAAGGG TTTTTTTCAG GCTGCGGGTC GGAGGGCAGA AGTGCAGTTC CCAGCCCAGA 1020
GACAGCGGGG CGGGTGGCTC TTCCTCACGC TCGCTCTTGG CTTGCTCCCT 1070