EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-08180 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr2:43400940-43402720 
Target genes
Number: 1             
NameEnsembl ID
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
AAAATTAGCT GGGCGTAGTG GCAGGTGCCC ATAATCCCAG CTACTTGGGA GGCTGAGGCA 60
GGAGAATGGC TTGATCCCAG GAGGCAGAGG TTGCAGTGAG CCGAGATTGC GCCATTGCAT 120
TCCAGTCTGG GCAACAAGAG GGAAACTCCA TCTCAAAAAG AAAAGAAAAA GAAATTCAAA 180
GGCAAGGTTA GACTGTCTCT TAACAGACTG GGGACAACCC CAAGAAATAA GAAGGCACCC 240
CCAGCCTCAC CTGTTATTTA CTTCTCAGAG CCTTCTGTGA GTCCAGCATT TGCAGGTCCT 300
GCCATGGAAG AAGCCGGCTC TGGGTGGACA AGCAGGAAGA CAGGAGGGTG GCCCTGGGTA 360
TACCATACCA CTGGGCTCAT GATATAGACC CCCCCAGTGG AAGGAAGCAA AGGAAAGACA 420
TTTCTGGGAC ATTTAGTGTA GGCCCAGCAC TGTGTTTTTA CAAGCGAGTA TTTTTGTTTT 480
TAATCTCAAC AACCCTATGA CTCCCATTTA TACAGATACA CCTCAGACCA GTGAAAAGCA 540
GTTAAAAGGC AGAGCCGGCA CTTAAACTTG ACCCCACAAC GTGGCCTGAT CTGTGTTCTG 600
GGGGTCTCCC CAGGCGCCGA GCTGCCAGGA GAAGGGTTGC CAGAGGGAAA GAGGAGGAGG 660
TGTTGGCCCA GCCCCCACAG CCCCAGCCCA GGCGAACATC CTCTCAGCCT GCCTTTATTG 720
TTCACAAAAC CGAAAAAGTG ATGATGGTTT TCCTTCCTCT CTTTAAGAAA ACAACAGAAT 780
CAAAACAAAC AGAGAAGGGG AACTCCCCTC CTGTAGCTTT TGCCAGAAAT GAAAGGAAGA 840
AATAATCCCC GTCATGACCT GGGCCGCCTC ACTGCTGCAA CAGGGTCTGG GAGGGGAAGA 900
GAAAAACCCC TGCCCCCCGA CCATAAAACC CAGAGTTTCT GCTTCCTGAT ACTGATACAA 960
GCTCAACCTC ACCCCCAGCA AATCCCTCAC TGTCCTCTGT CCATCACCTC ACACCGAAGA 1020
TCTGACACAC ACACACACAC ACACACACAC ACATACACAC AGCTGAAGCA GCTGAAACTT 1080
CCCAAAGAGC TTTAGTAAAT CCTAAGGAAG GGCAAAGAGG AAATAAAAAC ATACAAGTCC 1140
AGGAAATAAA AACAGCCCTC AAAATGCATT CCAGCATGTT TGACCCCCCA TAGTCACTTC 1200
CCACTTGAGG CTCCCAGGTC CTACCCCATT TCTCACTCCA GAGCTACCTG CACTGAGGCC 1260
CCCAAAGGAC TAGAATAGCC TCACAGGGTC CTTTCCAAGC TCTAGATTTG GGCTTGCCTG 1320
TATCTCAGCT GCCTCAACAA TCAAAGTCTA GAGCAGCGTA GAGCTTATGG TAATACAGGA 1380
CACCAGATCC CATCCTCACA GGAGCCCTCT CATTCATAAC TTAATATAGC TTTTAATTCC 1440
AGATAGCTTG TGCTGATTGG CTCACTTGGA GTGACTGGCA GCCTTCAGAG ATCACTCTGT 1500
CCACAGTACA CAGGGTTGTG GCCTTAAAGG CTCAGCAAGG TCATCATTTC TGAGCCTACA 1560
GTAACAGCCC TGTGGTCTCA CAGAATGGGA CCACCTGGTC AGCCTCATTC TTTAACAGGG 1620
ACTCTAGGGC CCATAGCACC TTTTGAAAAC TTCTGGATAA ATTAAGGAAT TTGTCTGTGG 1680
TCTGGATTCA AGGTCAGCGG GAGAACAGTT TTTCTCCATT ATTACTAATT AGCCTCAGCA 1740
AAGACTAAAT GACTACTTAG TAATATACTC AGTACTGTAC 1780