EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-13453 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:4076780-4078960 
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EsrraMA0592.2chr19:4078292-4078303GTCAAGGTCAT+6.32
EsrrgMA0643.1chr19:4078293-4078303TCAAGGTCAT+6.02
KLF16MA0741.1chr19:4077880-4077891GGGGGCGGGGC-6.02
KLF16MA0741.1chr19:4078493-4078504GGGGGCGGGGC-6.02
KLF5MA0599.1chr19:4077881-4077891GGGGCGGGGC-6.02
KLF5MA0599.1chr19:4078494-4078504GGGGCGGGGC-6.02
RARAMA0729.1chr19:4078295-4078313AAGGTCATGGGGTCAAGG+6.38
RREB1MA0073.1chr19:4077368-4077388GGGGAGGGGGTGGGTGGAGG-6.9
SP1MA0079.4chr19:4078492-4078507AGGGGGCGGGGCCAA-6.74
SP2MA0516.2chr19:4078491-4078508GAGGGGGCGGGGCCAAC-6.24
SP4MA0685.1chr19:4078490-4078507GGAGGGGGCGGGGCCAA-7.33
ZNF410MA0752.1chr19:4078468-4078485ACCATCCCATAATGTCC+6.84
ZNF740MA0753.2chr19:4078267-4078280GGGGGGGGGGGGG-6.03
ZNF740MA0753.2chr19:4078268-4078281GGGGGGGGGGGGG-6.03
ZNF740MA0753.2chr19:4078269-4078282GGGGGGGGGGGGG-6.03
ZNF740MA0753.2chr19:4078270-4078283GGGGGGGGGGGGG-6.03
ZNF740MA0753.2chr19:4078271-4078284GGGGGGGGGGGGG-6.03
Znf423MA0116.1chr19:4077739-4077754GGACCCCAAGGGTCA+6.01
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00556chr19:4077001-4079220Adipose_Nuclei
SE_00903chr19:4077001-4078985Adrenal_Gland
SE_02962chr19:4077722-4078869Bladder
SE_04051chr19:4077237-4078872Brain_Anterior_Caudate
SE_04973chr19:4076818-4078253Brain_Cingulate_Gyrus
SE_05886chr19:4076682-4079292Brain_Hippocampus_Middle
SE_06913chr19:4077245-4078884Brain_Hippocampus_Middle_150
SE_09464chr19:4076728-4079235CD14
SE_12453chr19:4077364-4078687CD3
SE_19502chr19:4077331-4078799CD4p_CD25-_Il17p_PMAstim_Th17
SE_20194chr19:4077093-4078799CD56
SE_22707chr19:4077085-4078881CD8_primiary
SE_23073chr19:4077156-4079002Colon_Crypt_1
SE_23728chr19:4077150-4078976Colon_Crypt_2
SE_24683chr19:4076954-4079045Colon_Crypt_3
SE_26455chr19:4077217-4078578Duodenum_Smooth_Muscle
SE_26575chr19:4076869-4078989Esophagus
SE_27700chr19:4077300-4079197Fetal_Intestine
SE_28696chr19:4077546-4078962Fetal_Intestine_Large
SE_31428chr19:4076846-4079073Gastric
SE_41127chr19:4076963-4079181Left_Ventricle
SE_42412chr19:4076855-4079136Lung
SE_48492chr19:4077467-4079202Psoas_Muscle
SE_48938chr19:4076994-4078953Right_Atrium
SE_50061chr19:4076798-4079480Sigmoid_Colon
SE_53358chr19:4076997-4079166Spleen
SE_55380chr19:4077588-4078419Thymus
SE_58113chr19:4077539-4078965VACO_9m
SE_59557chr19:4059049-4078953Ly3
SE_62529chr19:4051126-4090382Tonsil
SE_65287chr19:4076681-4078972Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1940770004078803
Number: 1             
IDChromosomeStartEnd
GH19I004077chr1940769994079016
Enhancer Sequence
CCATACTGGT TTCGAACTCC TGAGCTCAGG TGATCCACCC GCTTCGGCCT CCCAAAGTGC 60
TGAGATCACA GGCGTGAGCC ACCGTGCCCG GCCTGGGAGA AATACTTTCT GAGCTGCTGA 120
TTTCTCCATG GCTTCTGAAT TCATAGCGGT TGGGGAGATG GTGCCTGGGT ATTTTCACCT 180
GGGCAGCTGC TAAGAGGTGA CTTCTATTTG TTCCAGAAGA CAGAAGCCTT GGTAGCTATG 240
CTGGGACTGG ATCCGTGTCC ACCACACCAC TCAGAATTCC CATCTGCAAT GGGTCCCTTC 300
TGCCCCGTTT TTACCAAGCC CAGTTCCCTC TCTGCAACTG AGAGGCAGCC TCTTGCCCCA 360
CCCCCTCTCT TCCAGACTGG ATGGCTGCCT CCCAGGCACC TCTCAGGACC TGGCCACAGA 420
GCTCCAAAGC CCAGGGCCTG CTGCCTTTTG GGTCATGGCT CAGGGCCCAG TCTCTACCTC 480
TCTCTGTGGC CCAGTACCCT TTAGCTCAGG AGGTCTCATC TGGAGTGACT CTGCCTCCTT 540
CCAGGCGATA CTGGGTGATA TCTGGAGACA TTTTTAGGTG TTGTGATTGG GGAGGGGGTG 600
GGTGGAGGCC AGGGACACAG CTCAGCACCC TGCAGTGCCC AGGACGGACC CACCCCAGAG 660
GTTGATCAGG TCCCATAGTG TCCACCACAC CGAGGGGCTG AAATTCTAGC CTGGGTCTAA 720
CTTCAGTCTT GCTCGCTGTA GAAGGCACCC ACACACTTCT CTCCTCTCTG TGCTCTGCAG 780
AGAAGAAAAG CCACTGGCCA GTGACCCCTG GACAAGGCAG GACTTCAGCC ATCCACTGCC 840
CTCCACCACC ACCCCTGGGC ACCCCCTTGT CCAAAGCAGA CAGTCTCTAC TCTGGGATAA 900
GGGGGGGACC CTGGCCCCAG GCTTTACCCA CTTTGGGGTG ATTCCTGGAC CCTGGAGATG 960
GACCCCAAGG GTCACCCTCA CCCCACGGGA CCTCCCAACA ATGGACAAGG CCAGTCTGTC 1020
CTCTCCCCCA GCCCCCAGTT GTGCAGAATC CTCAACATGG CACCCCCAGT GTGGAGCTGA 1080
AGACTCCAGA CTTCAGGGGT GGGGGCGGGG CTGTGGGAGG GGAGATCATG GCTGCGGTTC 1140
TGGTCCAGCC AGACCTCCTG GGTTTGTTCT TTTTTTAAGA ACCACCGCAA TTTAAAGAGC 1200
GGAGTCCTCC CTCCCTGCAG CCCACCTGCC ACGTGGGCTG GCCCCTGTTC CCCTCTCCTT 1260
CTCTCCGTCT CTGCCTGCCG GGCTTGGGCT GCGGGGGCCG GAGCTTCCGT TTCACTTTGG 1320
TATCACCGGT TTCACTTTCA GGGCTGGGGA CAGAGAGAGG AGAAGAGGGA CAGAGAGATG 1380
GACAGAGCCG GGGAGGGTGG CCTTGTTAAG TCGGGGGCCG GGGAGGGGTC CACCACCTGC 1440
CGCTCCTTTT CCTGACCTTC CTGACCTTCT TCTGGCCTGG CCGGGGCGGG GGGGGGGGGG 1500
GGGGTCCTGG AAGTCAAGGT CATGGGGTCA AGGTCAAGTT CTCCCTGTGT GACCTTGGGT 1560
GGGAGAAGCA ACTTCCCACT ATCCCTGAGC CTCCTTTCCT GAACCCCTCA GTTACCCAAA 1620
AGTGGGGCTA AGAATCACGT ACACCCCACC CGGCGCTGGG AAGTTCAAAG ATTCCTCCAG 1680
CACCGCGGAC CATCCCATAA TGTCCCCGTG GGAGGGGGCG GGGCCAACTC CCAGGCAGAA 1740
CAGGATGTCG GCCGCTCCTT TGGCCAGGGA GAGACCCTTG GCCCAGAAAC CACCGGGAAG 1800
GAGGCTCCGG GCTGCCCGAG TCCCGAGCCC GGGATGAGCC ACTGTCCCCC AGAACCCCCA 1860
GCGGAGGCTG GAGCTCTGTC CGCTAGCAGA TCCAGGCTGG AAATTCAGTT GGGCATGGCC 1920
TTGTCCCACC CCACCTCCAT CCCCACCCCA CCCTCAGGTC CTTCCTGCTT GGTGGGGGCC 1980
TGGGGCTTGA GCCACTCACT CAAGAGCAGG GACTGGGACC CACTGACCTC CCTGTCCCCA 2040
GCACCCCCAC AGGGCCCAGT CAAGGTGGGG CAGGTGCTTG GTGCTGGTCA GACAGGATAG 2100
GGGAGTGACC ATTTGCATGT CAATATCAAT AACATATCTC GGTAGAGATA GGCGGTTAGT 2160
CTGTGTCAAA ATGTGAGAGG 2180