EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-25441 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr9:134127270-134129950 
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
TTACAGGCAT GAGCCGTGGC GCCCAGTCAA GAAAACCATT TTATCATCCT GTTACAACAA 60
GGTCAATAAT AGGTGTTAGC TATTGGCGGT TCTGTGCTGA GGGCCTTGCC TGATGACCCC 120
CCGGAACCCT CCTCCCTGTG AGGAAAGCGT AACCCTGTCT TGCAGATGAG GAAACCGAGG 180
CTCAGTGGTG CCGCCGAATC ACTCGGATTT GCTAAGCGCT TACTCTGGGC TGGGCACTTG 240
TCCAGAAGCT CAGGACCATC GGCTTCACGT GCCTCCGCAA TCTCGTGAGG TGAGGAACCA 300
CCTCCGTCCC CACTCCATGT CCTAGGAAAC CGAGACCTGA GAGGAGGGGG ACTTGCTCAA 360
GGTCACAGCC GTAGAGGCAC CGCCCGCCCA GGAGGGCTCA CATGACCCTC TCCGGCCTCC 420
AGGCCCAGCT GCAAGAGGAA GCACCGTCCT GGGGAGCCCG GAGACCCAGG CCCCCCTCAC 480
AGGCGAGGGG CTGGCACGCG GCCTCTGGAG GAACTTCTGG CCTTCACCGT CTCCGCCTGG 540
TCACTCGTCA ATGGCCGGCT GCCTTCTGGA AAGCTGCTGC TGCGCGACAG TGACCCTGGG 600
TGGAGTGAGG CATCCACGGG TGCTCGCTCC CAGAGATGGA GGCCGGAGCC CTGAGCAGAG 660
GCGCCGGCTG TGCCCCGGTC CTCTGTGGCC CCCAGGGCTG CAGAGCTGGG CAGGTCGATT 720
CCCTTGTCAC TCCTAAAAGA ACATTTGAAG CCCCCAGCAG GCTGGTGTGG GCACCCCAGT 780
TCCTCAGCTA CTCTGGGCTC TCCTTCCCCA GAGGCTGTGG GACCTGCCTT CCGGCCTCCG 840
TCACATGACC GCACAGCGAG GAGGCGCTTC TGTGAACCAG GAGGTGGCCC TCACCACGCA 900
GAAACTGTGG GCGCCTTCAT CTTGGACTTC CAGCCTCCAG AACTGTGAAG GATTGGTTTC 960
TGTGGTTGAC GAGGCATCCG GTCTATGGTT ACTTTATTCT AGAGCCCAAC TGGGCCAAGG 1020
TGATTGTACG TATCTGTGAA TATACTAAAA CCATAGAACC GTACACTTTC TATTTGCTTT 1080
TATTTTGTGA GACAGGGACT CACTGTCGCC CAGCTGGAGT GCGGTGGCAC GATCAGGGCT 1140
CGCTGCAGCC TCGACCTCCC ACCTCATTCT CCTGAGTAGC TGGGATGACG AGAATGTGCC 1200
ACCGCGCCCA GCTAATTTTT GTTGTTGTTG TTAGCTTTTT GAGATGGAGT CTCACTCTGT 1260
CACCCAGGCT GGAGTGCAGT GGCACAATCT CGGCTCACTG CAACCTCTGC CTCCCGGGTT 1320
CAAGCAATTC TCTGACTCAG CCTCCCGAGT AGCTGGGGTT ACAGGCGCCC GCCATCACAC 1380
TCAGCTAATT TTTGTATTTT TAGTAGAGAC AGGGTTTCTC CCTCTTGGCC AAGCTGGTCT 1440
TGAACTCCTG ACCTTGTGAT CCACCTGCCT CAGCCTCCCA GAGTGCTGGG ATTACAGGCA 1500
TGAGCCACTG AGTCTGGCCT ATGCCTGGCT AATTTTTAAG TTTTTTTGTA GAGATGGGGT 1560
CTCACTATGT TGCCCAGGCT GGTCTCAAAC TCCTGAGCCC AAGATCCTCC CACTTCGGTC 1620
TCCCAGAGTG CTGGGATTAC AGGCAGGAGC CACTGCACCG GCCAGAACCG TACACTTTTT 1680
TTTTTTTTTT TAAATGGAGT CTTTGTCACC CAGGCTGGAG TGCAGTGGTG CAATCTCACT 1740
GTAACCTCTA CCTCTCAGGT TCAAGTGATT CACCTGCCTC AGCCTCCTGA GTAACTGGGA 1800
TTACAGGCGT GTGCCACCAT GCCCTGCTAA TTTTTGTATT TTTTTCAGTA GAGACAGGAG 1860
TTCGCCATGT TGACCAGGCT GGTCTTGAAC TCCTGACTTC AGGTGATCTG CCCGCCTTGG 1920
CCTCCCAAAG TGCTGGGATT ACAGGCAGGA GCCACCACAC CCAGCCAGAA CCGTACTTTA 1980
AATAGGTGAG TTGTGTGGTA TGTGAACTGT ATCCCAATAA AGCTGAGGTA AAGCATTTTA 2040
ATACGTTTGT GTGACTGTCT GACCAGCATT CAGTCTGCAT TTGTCATGGA TGCTGAGAAT 2100
CCCACATCAC TAAGCCAGGC CCCTGTGGTC TAGATGTTGC AGAAGAATTG AGCCGTATTT 2160
AGAGAGAAGA GTCCCTGGTC TCTGAGCTAA GCCCTGGTGC TCAGTGTGAT TATTCTGGGG 2220
GCTCCATTTG CATGTTTAAC ACGGAGCACA ACTGCTATGC CTTTGCTGGG CCCCGGACCG 2280
GGGAGGACAG GGTAAGTGTG CGTGTCTCTG GCCTGACGAT TAGGAAACTC AGGCATGTGA 2340
GGTTGAGCGA CAAGCCTGGC CTCACTCAGC AAGGCAAGTG GCAGCCAGGA ATAGTGCAGG 2400
GCTCCCAGCT GTGTCTGGCC CGCCGTAAAC ACCCACCCTT CTTCTGTCTG ATTGAAAAGG 2460
GAACATGAAA TAAGAACCAG GGCTCAGGCT GATACAGGAA CTAATCCTGC CTCTGCATTC 2520
CAAGTCGTGC CGTCTGGGCC TGAAGGGAGC TGGGCTGGCC TTCGCCAGTT CCCATGTTGA 2580
TTTCGGGTTC ACCTCCCTGC ACACAGGCAC AGAGATGGAG TTCATTCACT CCGACGTGTT 2640
CGCTTGCATT TAGTAGTTTC CATCGGCCGG GCGCAGTGGC 2680