EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-58992 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr9:134130740-134132390 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr9:134130990-134131005TGAACTCCTGACCTC-6.22
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_09361chr9:134126808-134138940CD14
SE_10759chr9:134130225-134133328CD19_Primary
SE_11405chr9:134127138-134155283CD20
SE_12146chr9:134130208-134133493CD3
SE_13249chr9:134131782-134132497CD34_Primary_RO01480
SE_13579chr9:134131058-134133449CD34_Primary_RO01536
SE_14464chr9:134130006-134133411CD4_Memory_Primary_7pool
SE_15482chr9:134130757-134132926CD4_Memory_Primary_8pool
SE_15960chr9:134130241-134133433CD4_Naive_Primary_7pool
SE_16450chr9:134130517-134133034CD4_Naive_Primary_8pool
SE_17086chr9:134130919-134132783CD4p_CD225int_CD127p_Tmem
SE_17445chr9:134129893-134155392CD4p_CD25-_CD45RAp_Naive
SE_17921chr9:134128949-134133914CD4p_CD25-_CD45ROp_Memory
SE_18747chr9:134130406-134134742CD4p_CD25-_Il17-_PMAstim_Th
SE_19407chr9:134130269-134134369CD4p_CD25-_Il17p_PMAstim_Th17
SE_20268chr9:134127140-134134040CD56
SE_20819chr9:134130581-134133004CD8_Memory_7pool
SE_21594chr9:134130488-134133494CD8_Naive_7pool
SE_22019chr9:134130594-134133078CD8_Naive_8pool
SE_22737chr9:134130058-134134193CD8_primiary
SE_25701chr9:134127131-134134558DND41
SE_29891chr9:134130804-134132623Fetal_Muscle
SE_31045chr9:134130157-134132601Fetal_Thymus
SE_40648chr9:134130930-134132557Left_Ventricle
SE_42331chr9:134128984-134132556Lung
SE_43702chr9:134130117-134133808MM1S
SE_48088chr9:134128832-134130934Psoas_Muscle
SE_48088chr9:134131013-134133521Psoas_Muscle
SE_48582chr9:134128933-134132591Right_Atrium
SE_49606chr9:134131461-134132254Right_Ventricle
SE_50385chr9:134129114-134130941Sigmoid_Colon
SE_50385chr9:134130947-134132571Sigmoid_Colon
SE_51267chr9:134128852-134132710Skeletal_Muscle
SE_52980chr9:134130138-134130939Small_Intestine
SE_52980chr9:134130955-134132577Small_Intestine
SE_53628chr9:134128994-134133668Spleen
SE_55150chr9:134130163-134130946Thymus
SE_55150chr9:134130991-134132503Thymus
SE_59220chr9:134127420-134154306Ly3
SE_61761chr9:134100900-134154925Toledo
SE_62280chr9:134108336-134154785Tonsil
SE_67312chr9:134130117-134133808MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9134131602134132161
Number: 1             
IDChromosomeStartEnd
GH09I131251chr9134126988134134384
Enhancer Sequence
AGGGCCTGCA AGCGCCACAG GCCATCACAC TTTTTTTTTT TTTTTTTTAG ATGGAGCCTC 60
ACTCTGTCAC CCAGGCTCTG GAGTGTAGTG GTACAGTCTC GGCTCACTCC AACGTCTGCC 120
TCCTGGGTTC AAGCGATTCT CCTGCCTCAG CCTCCTGAGT AGTTAGGATT ATAGGCACCC 180
GCCACCATGC CTGGCTAATT TTTGTATTTT TAGTAGAGAC AGGGTTTCAC CATGTCGGTC 240
AGGCTGGTCT TGAACTCCTG ACCTCGTGAT CCACCCACCT TGGCCTCCCA AAGTTCTGGG 300
ATTACAGGCG TGAGCCACCG CACCCCGCCA GGCCATCAGC TTTTTTGTTT CCTGATGAAA 360
CTGTCTTCTT TTGGGCTCCA AGAGGGGCTT TCCTGTTTGG CCTCATGGCC CAGACTACAG 420
CAAGTCTCTG TCCCATTTAA AACAGCCCCA GAGCAGAAGA GGCTCTCCTG AGAAGTGACT 480
TTGAAAGTGG GAGGTGGAGA TGTTATGGGG TCGCTGTGCA GCTGCTTCTC CCAGACCCTG 540
GATGTCTCAG GCAGGTGAGC CTGGCCTGGC CCAGACAGCC GGCTCTCCCA GGCCCAGATC 600
CTGGAGAGGA ACCCGTGACA GCTGGGCAGA ATCTACTGTC TGTGCCTCTT CTCCCAGTCT 660
GGACTTCTAA ATTTCACCTG CTGTCAGCTG GAGAGGCTGG AGGGCTTCCA CTCTGTGACT 720
AAATGCCACT TGGAATCCAC TTTACTCACA ACTCCCTCCT TGTACATTTC CCTCTCGAAA 780
CTGTTACCCA CAGATTCAGC TGCGTCTCCC CATCTCCCGT CTCACTGCGC CTCTGCATGA 840
AGGCTTTGCT CTCCTGAGCT TCTGAAACCC TGCTATCAGG TTAGGCCTGC ATCCCATTCT 900
CTGTACACAC ACACACACAC ACACACACAC ACACACACAC ACACACACAC ACACACACAC 960
ACACACACCA TAGTCTCTCA TGGGCAGAGC TCAGGAGCCG ACTCCACACC GAGAAGCCAA 1020
ACCACGACAG TGAACTGCAC CACCCAGGAG CCATCTGCGT GGAGCTCGGC CAGCAATGCC 1080
TGTTATGCAA TTTCCTGCTT TGGTGTCTCA GCCCCAGGAG GCAGGATGTG AGCGCCGTTG 1140
GTTTGCTGCA ACGTGGAGAA CCCACAGAAG ACCCGAATTC TGATGCCCAG AGTGCATGGG 1200
GCCTCCCTGT CCCCGTGGGG GTGCAGAGAA GCCACTGCCC ACCCTGGATG ATGAGCCTGT 1260
GTGCGGTGGG TGCAGCAGCC GGCCCCTGCT CAAAGGGAAT CAGATGGGCT CATTGTGGGC 1320
CAGAAAGAAC TGACTGCCCC GAGACTTCCG GGGTGGGGAG GGGGGTGCAC TTCCTGCCCG 1380
GGGCACCCAG GATGGGGGAG CAGAGGCCTG GGACCTTCTC AGTAACAGTC ACCAATGTTA 1440
TTGGACACTG CACATGGCCC CACCGTCTCA GGCTCAAGAC TGAGAGTGCG CTATGGCGAG 1500
AGGTGGCTCT GTGGCCAGAG TTCGAATCCT GGCTCCGCCT TCCCCTAGCT ATGTGGTCTC 1560
AGGCAGCTCC TTGGCGTCCA CTCTCCCCGT TCCTTCGTCT GTGAAATGGG GGTGGCAGTT 1620
AACACCTCCC TTGTGGGGTT GTCATGAGGA 1650