EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS010-03633 
Organism
Homo sapiens 
Tissue/cell
B_cell_blood 
Coordinate
chr5:131760150-131761290 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10076733chr5131760731hg19
Number of super-enhancer constituents: 54             
IDCoordinateTissue/cell
SE_00037chr5:131744052-131766081Adipose_Nuclei
SE_01257chr5:131760302-131761260Adrenal_Gland
SE_02141chr5:131760114-131761327Aorta
SE_09163chr5:131754698-131768049CD14
SE_10413chr5:131754780-131764629CD19_Primary
SE_10915chr5:131741116-131769232CD20
SE_11905chr5:131759437-131767697CD3
SE_13055chr5:131759947-131760938CD34_Primary_RO01480
SE_13453chr5:131754417-131768040CD34_Primary_RO01536
SE_14162chr5:131757793-131764759CD34_Primary_RO01549
SE_14574chr5:131754589-131769241CD4_Memory_Primary_7pool
SE_15597chr5:131760276-131765055CD4_Memory_Primary_8pool
SE_16378chr5:131760280-131765089CD4_Naive_Primary_8pool
SE_17012chr5:131759982-131765601CD4p_CD225int_CD127p_Tmem
SE_17470chr5:131754338-131768227CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131754003-131768718CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131754349-131769426CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131758066-131768041CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131754313-131769496CD56
SE_20885chr5:131754675-131766460CD8_Memory_7pool
SE_21663chr5:131760036-131765468CD8_Naive_7pool
SE_22150chr5:131760173-131766300CD8_Naive_8pool
SE_22284chr5:131754357-131780344CD8_primiary
SE_23079chr5:131757777-131765509Colon_Crypt_1
SE_23750chr5:131760131-131761302Colon_Crypt_2
SE_25340chr5:131744602-131768034DND41
SE_25784chr5:131758078-131768069Duodenum_Smooth_Muscle
SE_26597chr5:131760116-131765409Esophagus
SE_27859chr5:131757729-131766672Fetal_Intestine
SE_28909chr5:131757525-131766711Fetal_Intestine_Large
SE_30917chr5:131758162-131767980Fetal_Thymus
SE_31393chr5:131757800-131765373Gastric
SE_32566chr5:131754945-131764808GM12878
SE_37471chr5:131760148-131766011HSMMtube
SE_39368chr5:131758209-131767951Jurkat
SE_40726chr5:131757690-131766735Left_Ventricle
SE_42103chr5:131757720-131766796Lung
SE_43553chr5:131754361-131767961MM1S
SE_45155chr5:131760166-131763941NHLF
SE_46095chr5:131759933-131765551Osteoblasts
SE_48659chr5:131760067-131761487Right_Atrium
SE_50034chr5:131757766-131768037RPMI-8402
SE_50051chr5:131757730-131767792Sigmoid_Colon
SE_52336chr5:131757743-131768421Small_Intestine
SE_53285chr5:131757733-131765501Spleen
SE_54554chr5:131758856-131766307Stomach_Smooth_Muscle
SE_55171chr5:131760917-131765208Thymus
SE_56265chr5:131760018-131765882u87
SE_59850chr5:131745223-131774088Ly4
SE_61542chr5:131744876-131774119Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131760262-131761285Pancreatic_islets
SE_66244chr5:131758209-131767951Jurkat
SE_67252chr5:131754361-131767961MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5131760381131760492
Number: 1             
IDChromosomeStartEnd
GH05I132418chr5131754337131769271
Enhancer Sequence
AGTGGTTAAG AGCATGGAAA AACAGATGTG GTACTGAGTG CCAGGTCCAC CTTTGCTAAG 60
TTTGTCACTT TGGGCATGTC CCCTAACCAG CCTGTTCCAC AGTTTCCTCA TCTGAGAATG 120
GGTATGAAAA TAGTAGCTAC TGCAAAGGGT GCTGTGAGAA TAAATATGAT AATGCACCCA 180
ACACAATTCC TGACCCAGAG TACAGCCTCC CTGAAGGTCA GCTGTAATGA TTGTGATATG 240
TAATGATTCC CACCCAACAG GCAGGAGAGC CTAGACCATG GAGGCTAGGT GACTTGCCTA 300
TGGTCACCTG ATAAAGCCAG AGATAGAAGC CAGGGCTCAT GGAGTCCCAG GCCAGTGGTC 360
TTTCCCCAGG ATTCCTGTTG TTTTTTAGGA GGAAATGTTA ATATAGACAG TTCTGTCTGT 420
GTCTAACCCC TTAGTAGCTG GTTCTGGCTT TTGTAGGGGA TTGGGGGACA GGACTTCCTC 480
AGCACACAAG ACCCTCAATC CTAGGCATTA GCCCCTCTGG GTGGGGCATT TGTGGGAGCA 540
GGGGACATGG CATGACTCCC TCTTTGTTCT GTGAGAGGCA GAGGGGGTTA GGAGTGCTGT 600
GCTCCCAGGA CTCTCCTCCT CCCACCGCCA CCTGCTGCCT GCCAGATCCT GTAGTCCTTC 660
CTGGGGAATC ATCACAGAGG CCTCCAGGAA CCTGGAGTGG GGAGGGAGCA GGACAGGCAG 720
GTCCTCCCTC CTGTGGCAGG ACTCTGTGGC TCAGGCCTGG GAACTGAGTG TGGGAGGAGG 780
TATGGTCTCC CTAAATAGTT GCTCCCAGCG GGCCATTTGG AAAGAGAAAC AGACTTTTGC 840
GCTAGGGGGC AGGGGCATAG ATACCCTCTG CAGCTGCCCT GGTCACCTTG TTGCCTGAAG 900
ACTGTTCCCA GTGGTCTTAG ATACAGAGTG GTGGCCCTTG CTCCTGTCAG AGTAGGTTTA 960
AAGACCACAC AGGTAGATTT CTCCCAGAAA CAACACCACT TAGAATTTTC CTTCAGGGAG 1020
CATAGCACAG GGGAGATGTC CACACACAGT CATACCTGTG TTTGAATCCC AGCTCTGCCT 1080
TTTTGCTTGT GGGTGGTCGA GTTGGGAGTG TGCTTGAGAA ATTATTCAGC CTCTTCAACT 1140