EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS010-00544 
Organism
Homo sapiens 
Tissue/cell
B_cell_blood 
Coordinate
chr10:11219460-11221170 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata4MA0482.1chr10:11220715-11220726AGGAGATAAGA-6.14
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_04267chr10:11204590-11222776Brain_Anterior_Caudate
SE_08093chr10:11216596-11225140Brain_Inferior_Temporal_Lobe
SE_09167chr10:11201519-11230155CD14
SE_10608chr10:11216500-11223017CD19_Primary
SE_11832chr10:11216422-11223661CD3
SE_12864chr10:11216593-11222843CD34_Primary_RO01480
SE_13327chr10:11203755-11226589CD34_Primary_RO01536
SE_14075chr10:11205099-11223264CD34_Primary_RO01549
SE_14387chr10:11216551-11223305CD4_Memory_Primary_7pool
SE_15413chr10:11217214-11222869CD4_Memory_Primary_8pool
SE_15818chr10:11220148-11222381CD4_Naive_Primary_7pool
SE_16289chr10:11216401-11222934CD4_Naive_Primary_8pool
SE_16868chr10:11216504-11223187CD4p_CD225int_CD127p_Tmem
SE_17335chr10:11202788-11227017CD4p_CD25-_CD45RAp_Naive
SE_17769chr10:11202533-11226312CD4p_CD25-_CD45ROp_Memory
SE_18233chr10:11202554-11236023CD4p_CD25-_Il17-_PMAstim_Th
SE_19105chr10:11216509-11226758CD4p_CD25-_Il17p_PMAstim_Th17
SE_19983chr10:11202622-11226777CD56
SE_20754chr10:11216298-11223105CD8_Memory_7pool
SE_21468chr10:11216634-11222889CD8_Naive_7pool
SE_21954chr10:11216648-11222888CD8_Naive_8pool
SE_22303chr10:11202099-11227377CD8_primiary
SE_25498chr10:11203315-11222915DND41
SE_26330chr10:11204115-11222628Duodenum_Smooth_Muscle
SE_31019chr10:11217089-11222875Fetal_Thymus
SE_32570chr10:11204380-11223175GM12878
SE_39428chr10:11214498-11224782Jurkat
SE_41283chr10:11219383-11222789Left_Ventricle
SE_43285chr10:11219450-11222689Lung
SE_43524chr10:11201953-11223381MM1S
SE_50008chr10:11215992-11222506RPMI-8402
SE_50505chr10:11219300-11221135Sigmoid_Colon
SE_52780chr10:11219401-11221040Small_Intestine
SE_53686chr10:11219334-11222943Spleen
SE_55145chr10:11219400-11220951Thymus
SE_62243chr10:11182932-11223246Tonsil
SE_66312chr10:11214498-11224782Jurkat
SE_67166chr10:11201953-11223381MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr101122057911221039
Enhancer Sequence
CAGTGAAGAA ATGTTGCTTA ATTTGTACAC TTCCCTGCAG TGCTGGAAAT GGACTTTTCC 60
TTTGCATTTC CATGAGTCAG GGAGAAAACA GACCAGCCTG GTTTCACGTT CCAGACAGCA 120
TGAAGTACCT CAACAGCAAA GAAGGAAATA GGGGCCTTAG TTTTTAAATC CTCTGTAAGA 180
TAGTCAAGGC TTCTCCAGTA GAAAGTTAGG TTTTGTAATA AGGGACCATT TTGTCCTTTC 240
TGTTCAGGAT TCAACAATTG CTTGTTGATT TGGGGTGAAG ATGCCATGAA CTCAGGAGCG 300
GGTGAGGAGG GCCTTTCTCT GCCTCCCATT CCCAAAGCAT TCTCCCTAAC CCCATGGTGG 360
AGGCTGCGGA GAGTGTTGTA GGCAGTTGCA GTGCCCGTCA CTCTCTGGGT GAAGCCAGTA 420
TGTCCTGGTG GTGGCCTTAG AAGACAGCCC CTGTGAGGCT CAGTAAGCCG CAGCCTAGAT 480
TGGAACAGCG TGACTGCCTG GTAGGATAAA GGAGACGACA TCTGAAAAGA GGGTTTCAGG 540
TGTTTGCAAA GAGGTCAGAT CCCTACACAT GAAACGCTGC GGCCACAGCT GCAGCCATGC 600
TACCTGCCAC ATGCCCTGGC CTGCGTCAGC GTTATGGAGT AGGCAACCTG GTTCGGCGCA 660
AAGAGGAAAT GCGCGTTCTG TGCCCAGTCC TCGCTCCCCT TTGCCAACCG GGCTGCTGAG 720
TGTGATGCTC CCTTTGTGAA GTGGACATCT GTCTAATGGG AACTGGACGG TGACCACCAG 780
TCCGTTTTAC ACAGGCCACC ATACAGCTGC CAGGTGGCGC TGGCTCTTAG CTGTTCTGCA 840
AGTCCAGCAC AGGGTGTATT CAGCTCTAGA GGTGGCAAAC ACGGGGCCCT TCCACCAGGC 900
CCACTCCCTG CAAAGGAAGT GCTTCCGAGA GCCAAGGCTT TGCTCTAATC TCTGTGAAGG 960
AAGAAAAAGA CTTGGGGAAA GGTAATGAAT AAATTAAAGA CACACTTTTG TAATCGTATA 1020
TTTTAGGCTT TCCTCTCTAC CTAATTGTGC TCTAATCTGT ACTTAGGAGT ATAGTTTTTT 1080
AAGTGGGACA TGTCAGGCTT TTATGCCACA GATTAAACTC CAAGGCAAAT AAATGTGTGA 1140
CAGCTTAAGA GGCGAAAAGA AGAGTCTTCG TCAAATGGCA GAGTTTGATT GTTTAACCTA 1200
GACTAATCAG TCTTTGGAGG GCCTGCCACA TGTCTTCCAG ACGGCTAGAA TGCTCAGGAG 1260
ATAAGAGTGG GGCCTATCGC TCTGTGGCTT TCTCCCCCTG CATTAGCCGC AGAGCTGAGT 1320
GAGTCTATGA AAACCCATTG GTCGGGCTGC CCTAGCAACA CAGAATGCTG TGCTGACACA 1380
TACTCCATCA CATGTTTGCG ATGAAAATGC TGTATTTTTA GAACACTTCA AAGTCAGGAA 1440
ACCGTTAAAC CACACTGCAT CCTCTCTTGC CCTCTGGCCA CTTCCTCCAC ACCCCCAGGA 1500
ACATTGCCCC CATTTCACAG AAAAGGAGCC TGAGACAAAG ATTAAGTGAT ATTTTAAGCA 1560
AAGCTGATAA TCCCAGGGAA AATTGCTGAT CAAGTCTTGA AATCCAACAC ATCCTTCGGA 1620
GTAATTTTTA ATGCTTTCGC TTCTTTTACC TAAGCCATGT GTGTTCCATA TGACCTTAAA 1680
TCTAAGCCCT AATATTGTAA ATGGAGTTCA 1710