EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-12133 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr2:43400480-43403130 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
LHX6MA0658.1chr2:43402663-43402673ACTAATTAGC+6.02
NFYBMA0502.1chr2:43402392-43402407CTGATTGGCTCACTT-6.96
Nr5a2MA0505.1chr2:43402623-43402638GGATTCAAGGTCAGC+6.53
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_03102chr2:43401820-43402633Bladder
SE_09287chr2:43400075-43403682CD14
SE_10736chr2:43400302-43403389CD19_Primary
SE_11722chr2:43394406-43403989CD20
SE_11879chr2:43400091-43404148CD3
SE_13409chr2:43400938-43402603CD34_Primary_RO01536
SE_14384chr2:43400219-43408412CD4_Memory_Primary_7pool
SE_16107chr2:43400099-43403788CD4_Naive_Primary_7pool
SE_16655chr2:43400130-43404267CD4_Naive_Primary_8pool
SE_16950chr2:43400244-43403998CD4p_CD225int_CD127p_Tmem
SE_17323chr2:43394585-43404415CD4p_CD25-_CD45RAp_Naive
SE_17875chr2:43395625-43407220CD4p_CD25-_CD45ROp_Memory
SE_18565chr2:43400105-43406913CD4p_CD25-_Il17-_PMAstim_Th
SE_19552chr2:43400302-43404154CD4p_CD25-_Il17p_PMAstim_Th17
SE_20209chr2:43400106-43404112CD56
SE_20901chr2:43400086-43404285CD8_Memory_7pool
SE_22349chr2:43400041-43404227CD8_primiary
SE_23059chr2:43401721-43402635Colon_Crypt_1
SE_23724chr2:43401426-43401722Colon_Crypt_2
SE_23724chr2:43401742-43402619Colon_Crypt_2
SE_25333chr2:43400942-43403313DND41
SE_26374chr2:43400976-43403020Duodenum_Smooth_Muscle
SE_26557chr2:43401076-43402726Esophagus
SE_27617chr2:43401083-43402573Fetal_Intestine
SE_30898chr2:43400975-43402804Fetal_Thymus
SE_31392chr2:43400996-43402742Gastric
SE_38828chr2:43400455-43403357HUVEC
SE_40066chr2:43401109-43402352K562
SE_40066chr2:43402488-43403348K562
SE_43203chr2:43400997-43403305Lung
SE_49954chr2:43401006-43403268RPMI-8402
SE_50052chr2:43400989-43403336Sigmoid_Colon
SE_52337chr2:43400377-43400975Small_Intestine
SE_52337chr2:43400999-43403398Small_Intestine
SE_53288chr2:43400358-43403248Spleen
SE_55101chr2:43400499-43400884Thymus
SE_55101chr2:43401055-43402473Thymus
SE_58412chr2:43352450-43425007Ly1
SE_61450chr2:43354337-43468354Toledo
SE_62203chr2:43354169-43468733Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr24340062143402630
chr24340153543402035
Number: 1             
IDChromosomeStartEnd
GH02I043167chr24339474143409195
Enhancer Sequence
ATTTTAAAAG TACAAGTACT GCCACAGAGT GCAGGTCTGC AAAGTGTTTC GACTCTACAA 60
AAGAGTGTTT GTATTTTAAA AGTTCAGGAA CCATTTTACG GACTAAGACA CTGAGGCCCT 120
AGGAGATAGG GCTTCTTGGC CAAGTTGCAG AGCCAGCTGG GGCCCAGGGA GTTTAATCCA 180
AGTGGTGTGG GTCTCCCTTT CTCTCTGTTC AGGGAAGTGC CCCCTTCATC CCCTCAGAGA 240
AGGGCCCCAG GACTGCAGGA CAGGCCATGG GGGGTGCAAC CTTGGGAGGC ATGAAGCTTG 300
AGGAACTGAA GGGCTAGGAG AAATTCAAGG GCTGGGCACA GTGGGTCACA CCTATAATCC 360
CAGCATTTTG GGAGATCAAG GCAGGTGGAT CACCTGAAGT CAGGAGTTCA ACACCAGCCT 420
GGCCAACATG GTGAAACCCC GTCTCTACTA AAAGTACAAA AAAATTAGCT GGGCGTAGTG 480
GCAGGTGCCC ATAATCCCAG CTACTTGGGA GGCTGAGGCA GGAGAATGGC TTGATCCCAG 540
GAGGCAGAGG TTGCAGTGAG CCGAGATTGC GCCATTGCAT TCCAGTCTGG GCAACAAGAG 600
GGAAACTCCA TCTCAAAAAG AAAAGAAAAA GAAATTCAAA GGCAAGGTTA GACTGTCTCT 660
TAACAGACTG GGGACAACCC CAAGAAATAA GAAGGCACCC CCAGCCTCAC CTGTTATTTA 720
CTTCTCAGAG CCTTCTGTGA GTCCAGCATT TGCAGGTCCT GCCATGGAAG AAGCCGGCTC 780
TGGGTGGACA AGCAGGAAGA CAGGAGGGTG GCCCTGGGTA TACCATACCA CTGGGCTCAT 840
GATATAGACC CCCCCAGTGG AAGGAAGCAA AGGAAAGACA TTTCTGGGAC ATTTAGTGTA 900
GGCCCAGCAC TGTGTTTTTA CAAGCGAGTA TTTTTGTTTT TAATCTCAAC AACCCTATGA 960
CTCCCATTTA TACAGATACA CCTCAGACCA GTGAAAAGCA GTTAAAAGGC AGAGCCGGCA 1020
CTTAAACTTG ACCCCACAAC GTGGCCTGAT CTGTGTTCTG GGGGTCTCCC CAGGCGCCGA 1080
GCTGCCAGGA GAAGGGTTGC CAGAGGGAAA GAGGAGGAGG TGTTGGCCCA GCCCCCACAG 1140
CCCCAGCCCA GGCGAACATC CTCTCAGCCT GCCTTTATTG TTCACAAAAC CGAAAAAGTG 1200
ATGATGGTTT TCCTTCCTCT CTTTAAGAAA ACAACAGAAT CAAAACAAAC AGAGAAGGGG 1260
AACTCCCCTC CTGTAGCTTT TGCCAGAAAT GAAAGGAAGA AATAATCCCC GTCATGACCT 1320
GGGCCGCCTC ACTGCTGCAA CAGGGTCTGG GAGGGGAAGA GAAAAACCCC TGCCCCCCGA 1380
CCATAAAACC CAGAGTTTCT GCTTCCTGAT ACTGATACAA GCTCAACCTC ACCCCCAGCA 1440
AATCCCTCAC TGTCCTCTGT CCATCACCTC ACACCGAAGA TCTGACACAC ACACACACAC 1500
ACACACACAC ACATACACAC AGCTGAAGCA GCTGAAACTT CCCAAAGAGC TTTAGTAAAT 1560
CCTAAGGAAG GGCAAAGAGG AAATAAAAAC ATACAAGTCC AGGAAATAAA AACAGCCCTC 1620
AAAATGCATT CCAGCATGTT TGACCCCCCA TAGTCACTTC CCACTTGAGG CTCCCAGGTC 1680
CTACCCCATT TCTCACTCCA GAGCTACCTG CACTGAGGCC CCCAAAGGAC TAGAATAGCC 1740
TCACAGGGTC CTTTCCAAGC TCTAGATTTG GGCTTGCCTG TATCTCAGCT GCCTCAACAA 1800
TCAAAGTCTA GAGCAGCGTA GAGCTTATGG TAATACAGGA CACCAGATCC CATCCTCACA 1860
GGAGCCCTCT CATTCATAAC TTAATATAGC TTTTAATTCC AGATAGCTTG TGCTGATTGG 1920
CTCACTTGGA GTGACTGGCA GCCTTCAGAG ATCACTCTGT CCACAGTACA CAGGGTTGTG 1980
GCCTTAAAGG CTCAGCAAGG TCATCATTTC TGAGCCTACA GTAACAGCCC TGTGGTCTCA 2040
CAGAATGGGA CCACCTGGTC AGCCTCATTC TTTAACAGGG ACTCTAGGGC CCATAGCACC 2100
TTTTGAAAAC TTCTGGATAA ATTAAGGAAT TTGTCTGTGG TCTGGATTCA AGGTCAGCGG 2160
GAGAACAGTT TTTCTCCATT ATTACTAATT AGCCTCAGCA AAGACTAAAT GACTACTTAG 2220
TAATATACTC AGTACTGTAC CTGGTCCTGT GGGAAATGTA CATATGAAGA TAGATGAGTC 2280
TCAAAGCCTC TCAGGGGCAA GAGAAGGATG GAGGCAGGGA GAGGTTTCTG CCTAAACAAT 2340
CAGAAAAGAG TCTATATGAA AACTCCTCTA AGAGCTGTTG GAGGGTTGGA GGGGATAAGG 2400
CAGCATGTGT GACATTGCTA ACTGTTTGAG GATTATGGAC CACAATGACC TGAGCTCCCT 2460
GAGGTCAGAA AATGTCTTGC CCCTTTTGGG TCTCAGGACT GATAGGTCCT GCACTTAGGA 2520
GGGGCTCAAT TGGCATCTGT TGGGTGAATC ACCATTTTCT GGCTTCACTG GCAGCAGATG 2580
GTCAGAGGAG GTCAAGCAAT GATTATTCTC CTGAAGAAGA GACCAGACCA GGGCTGAAGC 2640
CAGATCTTCT 2650