EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-41740 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr9:134127260-134129940 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr9:134128710-134128725TGAACTCCTGACCTT-6.04
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_09361chr9:134126808-134138940CD14
SE_10759chr9:134127597-134128798CD19_Primary
SE_10759chr9:134129071-134130092CD19_Primary
SE_11405chr9:134127138-134155283CD20
SE_12146chr9:134127388-134128667CD3
SE_13579chr9:134129040-134129863CD34_Primary_RO01536
SE_14464chr9:134127455-134128961CD4_Memory_Primary_7pool
SE_15482chr9:134127371-134128807CD4_Memory_Primary_8pool
SE_15960chr9:134127501-134128571CD4_Naive_Primary_7pool
SE_16450chr9:134127075-134129180CD4_Naive_Primary_8pool
SE_17086chr9:134127596-134128651CD4p_CD225int_CD127p_Tmem
SE_17445chr9:134127278-134128798CD4p_CD25-_CD45RAp_Naive
SE_17921chr9:134127143-134128818CD4p_CD25-_CD45ROp_Memory
SE_17921chr9:134128949-134133914CD4p_CD25-_CD45ROp_Memory
SE_18747chr9:134127276-134130091CD4p_CD25-_Il17-_PMAstim_Th
SE_19407chr9:134127352-134128974CD4p_CD25-_Il17p_PMAstim_Th17
SE_19407chr9:134129136-134129864CD4p_CD25-_Il17p_PMAstim_Th17
SE_20268chr9:134127140-134134040CD56
SE_22019chr9:134127263-134129043CD8_Naive_8pool
SE_22737chr9:134127230-134128886CD8_primiary
SE_25701chr9:134127131-134134558DND41
SE_29891chr9:134128784-134130563Fetal_Muscle
SE_31045chr9:134127465-134128619Fetal_Thymus
SE_31045chr9:134129107-134129947Fetal_Thymus
SE_40648chr9:134128980-134130844Left_Ventricle
SE_42331chr9:134127446-134128634Lung
SE_42331chr9:134128984-134132556Lung
SE_43702chr9:134126991-134129967MM1S
SE_48088chr9:134128832-134130934Psoas_Muscle
SE_48582chr9:134127408-134128623Right_Atrium
SE_48582chr9:134128933-134132591Right_Atrium
SE_50385chr9:134127192-134128724Sigmoid_Colon
SE_50385chr9:134129114-134130941Sigmoid_Colon
SE_51267chr9:134128852-134132710Skeletal_Muscle
SE_52980chr9:134127300-134128654Small_Intestine
SE_52980chr9:134129149-134130121Small_Intestine
SE_53628chr9:134127297-134128806Spleen
SE_53628chr9:134128994-134133668Spleen
SE_55150chr9:134127535-134128527Thymus
SE_55150chr9:134129107-134129693Thymus
SE_59220chr9:134127420-134154306Ly3
SE_61761chr9:134100900-134154925Toledo
SE_62280chr9:134108336-134154785Tonsil
SE_67312chr9:134126991-134129967MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9134128008134128436
Number: 1             
IDChromosomeStartEnd
GH09I131251chr9134126988134134384
Enhancer Sequence
AGTGGTGGGA TTACAGGCAT GAGCCGTGGC GCCCAGTCAA GAAAACCATT TTATCATCCT 60
GTTACAACAA GGTCAATAAT AGGTGTTAGC TATTGGCGGT TCTGTGCTGA GGGCCTTGCC 120
TGATGACCCC CCGGAACCCT CCTCCCTGTG AGGAAAGCGT AACCCTGTCT TGCAGATGAG 180
GAAACCGAGG CTCAGTGGTG CCGCCGAATC ACTCGGATTT GCTAAGCGCT TACTCTGGGC 240
TGGGCACTTG TCCAGAAGCT CAGGACCATC GGCTTCACGT GCCTCCGCAA TCTCGTGAGG 300
TGAGGAACCA CCTCCGTCCC CACTCCATGT CCTAGGAAAC CGAGACCTGA GAGGAGGGGG 360
ACTTGCTCAA GGTCACAGCC GTAGAGGCAC CGCCCGCCCA GGAGGGCTCA CATGACCCTC 420
TCCGGCCTCC AGGCCCAGCT GCAAGAGGAA GCACCGTCCT GGGGAGCCCG GAGACCCAGG 480
CCCCCCTCAC AGGCGAGGGG CTGGCACGCG GCCTCTGGAG GAACTTCTGG CCTTCACCGT 540
CTCCGCCTGG TCACTCGTCA ATGGCCGGCT GCCTTCTGGA AAGCTGCTGC TGCGCGACAG 600
TGACCCTGGG TGGAGTGAGG CATCCACGGG TGCTCGCTCC CAGAGATGGA GGCCGGAGCC 660
CTGAGCAGAG GCGCCGGCTG TGCCCCGGTC CTCTGTGGCC CCCAGGGCTG CAGAGCTGGG 720
CAGGTCGATT CCCTTGTCAC TCCTAAAAGA ACATTTGAAG CCCCCAGCAG GCTGGTGTGG 780
GCACCCCAGT TCCTCAGCTA CTCTGGGCTC TCCTTCCCCA GAGGCTGTGG GACCTGCCTT 840
CCGGCCTCCG TCACATGACC GCACAGCGAG GAGGCGCTTC TGTGAACCAG GAGGTGGCCC 900
TCACCACGCA GAAACTGTGG GCGCCTTCAT CTTGGACTTC CAGCCTCCAG AACTGTGAAG 960
GATTGGTTTC TGTGGTTGAC GAGGCATCCG GTCTATGGTT ACTTTATTCT AGAGCCCAAC 1020
TGGGCCAAGG TGATTGTACG TATCTGTGAA TATACTAAAA CCATAGAACC GTACACTTTC 1080
TATTTGCTTT TATTTTGTGA GACAGGGACT CACTGTCGCC CAGCTGGAGT GCGGTGGCAC 1140
GATCAGGGCT CGCTGCAGCC TCGACCTCCC ACCTCATTCT CCTGAGTAGC TGGGATGACG 1200
AGAATGTGCC ACCGCGCCCA GCTAATTTTT GTTGTTGTTG TTAGCTTTTT GAGATGGAGT 1260
CTCACTCTGT CACCCAGGCT GGAGTGCAGT GGCACAATCT CGGCTCACTG CAACCTCTGC 1320
CTCCCGGGTT CAAGCAATTC TCTGACTCAG CCTCCCGAGT AGCTGGGGTT ACAGGCGCCC 1380
GCCATCACAC TCAGCTAATT TTTGTATTTT TAGTAGAGAC AGGGTTTCTC CCTCTTGGCC 1440
AAGCTGGTCT TGAACTCCTG ACCTTGTGAT CCACCTGCCT CAGCCTCCCA GAGTGCTGGG 1500
ATTACAGGCA TGAGCCACTG AGTCTGGCCT ATGCCTGGCT AATTTTTAAG TTTTTTTGTA 1560
GAGATGGGGT CTCACTATGT TGCCCAGGCT GGTCTCAAAC TCCTGAGCCC AAGATCCTCC 1620
CACTTCGGTC TCCCAGAGTG CTGGGATTAC AGGCAGGAGC CACTGCACCG GCCAGAACCG 1680
TACACTTTTT TTTTTTTTTT TAAATGGAGT CTTTGTCACC CAGGCTGGAG TGCAGTGGTG 1740
CAATCTCACT GTAACCTCTA CCTCTCAGGT TCAAGTGATT CACCTGCCTC AGCCTCCTGA 1800
GTAACTGGGA TTACAGGCGT GTGCCACCAT GCCCTGCTAA TTTTTGTATT TTTTTCAGTA 1860
GAGACAGGAG TTCGCCATGT TGACCAGGCT GGTCTTGAAC TCCTGACTTC AGGTGATCTG 1920
CCCGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCAGGA GCCACCACAC CCAGCCAGAA 1980
CCGTACTTTA AATAGGTGAG TTGTGTGGTA TGTGAACTGT ATCCCAATAA AGCTGAGGTA 2040
AAGCATTTTA ATACGTTTGT GTGACTGTCT GACCAGCATT CAGTCTGCAT TTGTCATGGA 2100
TGCTGAGAAT CCCACATCAC TAAGCCAGGC CCCTGTGGTC TAGATGTTGC AGAAGAATTG 2160
AGCCGTATTT AGAGAGAAGA GTCCCTGGTC TCTGAGCTAA GCCCTGGTGC TCAGTGTGAT 2220
TATTCTGGGG GCTCCATTTG CATGTTTAAC ACGGAGCACA ACTGCTATGC CTTTGCTGGG 2280
CCCCGGACCG GGGAGGACAG GGTAAGTGTG CGTGTCTCTG GCCTGACGAT TAGGAAACTC 2340
AGGCATGTGA GGTTGAGCGA CAAGCCTGGC CTCACTCAGC AAGGCAAGTG GCAGCCAGGA 2400
ATAGTGCAGG GCTCCCAGCT GTGTCTGGCC CGCCGTAAAC ACCCACCCTT CTTCTGTCTG 2460
ATTGAAAAGG GAACATGAAA TAAGAACCAG GGCTCAGGCT GATACAGGAA CTAATCCTGC 2520
CTCTGCATTC CAAGTCGTGC CGTCTGGGCC TGAAGGGAGC TGGGCTGGCC TTCGCCAGTT 2580
CCCATGTTGA TTTCGGGTTC ACCTCCCTGC ACACAGGCAC AGAGATGGAG TTCATTCACT 2640
CCGACGTGTT CGCTTGCATT TAGTAGTTTC CATCGGCCGG 2680