EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS164-06788 
Organism
Homo sapiens 
Tissue/cell
Raji 
Coordinate
chr2:43400720-43403570 
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: 38             
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_52337chr2:43400999-43403398Small_Intestine
SE_53288chr2:43400358-43403248Spleen
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: 1             
ChromosomeStartEnd
chr24340153543402035
Number: 1             
IDChromosomeStartEnd
GH02I043167chr24339474143409195
Enhancer Sequence
AGGGCCCCAG GACTGCAGGA CAGGCCATGG GGGGTGCAAC CTTGGGAGGC ATGAAGCTTG 60
AGGAACTGAA GGGCTAGGAG AAATTCAAGG GCTGGGCACA GTGGGTCACA CCTATAATCC 120
CAGCATTTTG GGAGATCAAG GCAGGTGGAT CACCTGAAGT CAGGAGTTCA ACACCAGCCT 180
GGCCAACATG GTGAAACCCC GTCTCTACTA AAAGTACAAA AAAATTAGCT GGGCGTAGTG 240
GCAGGTGCCC ATAATCCCAG CTACTTGGGA GGCTGAGGCA GGAGAATGGC TTGATCCCAG 300
GAGGCAGAGG TTGCAGTGAG CCGAGATTGC GCCATTGCAT TCCAGTCTGG GCAACAAGAG 360
GGAAACTCCA TCTCAAAAAG AAAAGAAAAA GAAATTCAAA GGCAAGGTTA GACTGTCTCT 420
TAACAGACTG GGGACAACCC CAAGAAATAA GAAGGCACCC CCAGCCTCAC CTGTTATTTA 480
CTTCTCAGAG CCTTCTGTGA GTCCAGCATT TGCAGGTCCT GCCATGGAAG AAGCCGGCTC 540
TGGGTGGACA AGCAGGAAGA CAGGAGGGTG GCCCTGGGTA TACCATACCA CTGGGCTCAT 600
GATATAGACC CCCCCAGTGG AAGGAAGCAA AGGAAAGACA TTTCTGGGAC ATTTAGTGTA 660
GGCCCAGCAC TGTGTTTTTA CAAGCGAGTA TTTTTGTTTT TAATCTCAAC AACCCTATGA 720
CTCCCATTTA TACAGATACA CCTCAGACCA GTGAAAAGCA GTTAAAAGGC AGAGCCGGCA 780
CTTAAACTTG ACCCCACAAC GTGGCCTGAT CTGTGTTCTG GGGGTCTCCC CAGGCGCCGA 840
GCTGCCAGGA GAAGGGTTGC CAGAGGGAAA GAGGAGGAGG TGTTGGCCCA GCCCCCACAG 900
CCCCAGCCCA GGCGAACATC CTCTCAGCCT GCCTTTATTG TTCACAAAAC CGAAAAAGTG 960
ATGATGGTTT TCCTTCCTCT CTTTAAGAAA ACAACAGAAT CAAAACAAAC AGAGAAGGGG 1020
AACTCCCCTC CTGTAGCTTT TGCCAGAAAT GAAAGGAAGA AATAATCCCC GTCATGACCT 1080
GGGCCGCCTC ACTGCTGCAA CAGGGTCTGG GAGGGGAAGA GAAAAACCCC TGCCCCCCGA 1140
CCATAAAACC CAGAGTTTCT GCTTCCTGAT ACTGATACAA GCTCAACCTC ACCCCCAGCA 1200
AATCCCTCAC TGTCCTCTGT CCATCACCTC ACACCGAAGA TCTGACACAC ACACACACAC 1260
ACACACACAC ACATACACAC AGCTGAAGCA GCTGAAACTT CCCAAAGAGC TTTAGTAAAT 1320
CCTAAGGAAG GGCAAAGAGG AAATAAAAAC ATACAAGTCC AGGAAATAAA AACAGCCCTC 1380
AAAATGCATT CCAGCATGTT TGACCCCCCA TAGTCACTTC CCACTTGAGG CTCCCAGGTC 1440
CTACCCCATT TCTCACTCCA GAGCTACCTG CACTGAGGCC CCCAAAGGAC TAGAATAGCC 1500
TCACAGGGTC CTTTCCAAGC TCTAGATTTG GGCTTGCCTG TATCTCAGCT GCCTCAACAA 1560
TCAAAGTCTA GAGCAGCGTA GAGCTTATGG TAATACAGGA CACCAGATCC CATCCTCACA 1620
GGAGCCCTCT CATTCATAAC TTAATATAGC TTTTAATTCC AGATAGCTTG TGCTGATTGG 1680
CTCACTTGGA GTGACTGGCA GCCTTCAGAG ATCACTCTGT CCACAGTACA CAGGGTTGTG 1740
GCCTTAAAGG CTCAGCAAGG TCATCATTTC TGAGCCTACA GTAACAGCCC TGTGGTCTCA 1800
CAGAATGGGA CCACCTGGTC AGCCTCATTC TTTAACAGGG ACTCTAGGGC CCATAGCACC 1860
TTTTGAAAAC TTCTGGATAA ATTAAGGAAT TTGTCTGTGG TCTGGATTCA AGGTCAGCGG 1920
GAGAACAGTT TTTCTCCATT ATTACTAATT AGCCTCAGCA AAGACTAAAT GACTACTTAG 1980
TAATATACTC AGTACTGTAC CTGGTCCTGT GGGAAATGTA CATATGAAGA TAGATGAGTC 2040
TCAAAGCCTC TCAGGGGCAA GAGAAGGATG GAGGCAGGGA GAGGTTTCTG CCTAAACAAT 2100
CAGAAAAGAG TCTATATGAA AACTCCTCTA AGAGCTGTTG GAGGGTTGGA GGGGATAAGG 2160
CAGCATGTGT GACATTGCTA ACTGTTTGAG GATTATGGAC CACAATGACC TGAGCTCCCT 2220
GAGGTCAGAA AATGTCTTGC CCCTTTTGGG TCTCAGGACT GATAGGTCCT GCACTTAGGA 2280
GGGGCTCAAT TGGCATCTGT TGGGTGAATC ACCATTTTCT GGCTTCACTG GCAGCAGATG 2340
GTCAGAGGAG GTCAAGCAAT GATTATTCTC CTGAAGAAGA GACCAGACCA GGGCTGAAGC 2400
CAGATCTTCT ACCTCTCTGA GCAATCCCTT TTTCTCAGCA GCCTCAATGC CCCACTCAGC 2460
CTTCAACCTT TCTCAACTGA ACAGCAAGAT AGTTATCCTC CTTTGCATTG TGGCTTTTTT 2520
TTTTTTTTTT TCGAGACGGA GTCTAGCTCT GTCACCAGGC TGGAGTGCAG TGCGCGATCT 2580
CGGCTCACTG CAACCTCCAC CTTCTGGGTT CAAGCAATTC TGCTGCCTCA GCCTCCCAAA 2640
TAGCTCGGAT TACAGGCACG CGCCGCCACA CCCAGCTAAT TTTTGTATTT TTAGTAGAGA 2700
CAGGGTTTCA CCATGTTGGC CAGGATGGTC TTGATCTCCT GACCTCGTGC TCCACCCAAC 2760
TCGGCCTCCC AAAGTGCTGG GATTACAGGT GTGAGCCACT GTACCCAGCC TGCACTGTAT 2820
TTTTAATATA TTCTCCAAGT GGCCTCTGGA 2850